Canonical Allele Identifier: PA2826567561
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 422130
ClinVar Variation Id: 925213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Glu248Asp
CA001463
NM_001276761.3:c.744G>C
CA397836649
NM_001276761.3:c.744G>T