Canonical Allele Identifier: PA2826566558
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718262
ClinVar RCV Id: RCV002304859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro38Ala
CA397845624
NM_001276761.3:c.112C>G