Canonical Allele Identifier: PA2826559597
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406606
ClinVar RCV Id: RCV000462657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Asp145Gly
CA16615998
NM_001276695.3:c.434A>G