Canonical Allele Identifier: PA2826567386
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Glu219Asp
CA397837660
NM_001276761.3:c.657A>T
CA397837662
NM_001276761.3:c.657A>C