Canonical Allele Identifier: PA2826559278
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Leu91Pro
CA397842949
NM_001276695.3:c.272T>C