Canonical Allele Identifier: PA658679493
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458545
ClinVar RCV Id: RCV000527533 RCV001764539 RCV002341276 RCV003476227 RCV004023788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Ala27Val
CA397842017
NM_001126117.1:c.80C>T
CA645589022
NM_001126117.1:c.80_81delinsTT