Canonical Allele Identifier: PA2826560250
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 481049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro262Leu
CA397836344
NM_001276695.3:c.785C>T