Canonical Allele Identifier: PA2826566981
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137906
ClinVar RCV Id: RCV003064392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala150Asp
CA397840870
NM_001276761.3:c.449C>A