Canonical Allele Identifier: PA2826560142
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376658
ClinVar RCV Id: RCV000418465 RCV000419917 RCV000420625 RCV000421324 RCV000424417 RCV000427170 RCV000426479 RCV000430194 RCV000429590 RCV000431582 RCV000435565 RCV000436708 RCV000439619 RCV000438255 RCV000439812 RCV000439157 RCV000445156 RCV000568150 RCV000706131 RCV000785300 RCV003476010 RCV004022240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg241Gly
CA16603073
NM_001276695.3:c.721A>G