Canonical Allele Identifier: PA2826559928
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12355
ClinVar RCV Id: RCV000013149 RCV000419718 RCV000421831 RCV000426192 RCV000429017 RCV000436871 RCV000164465 RCV000422520 RCV000206683 RCV000440814 RCV000427250 RCV000432021 RCV000444212 RCV000431450 RCV000437916 RCV000439739 RCV000443515 RCV000421349 RCV000785472 RCV000444304 RCV000986053 RCV003473082
ClinVar Variation Id: 861760
ClinVar RCV Id: RCV001068346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Gly206Asp
CA000371
NM_001276695.3:c.617G>A
CA916081933
NM_001276695.3:c.617_618delinsAT