Canonical Allele Identifier: PA2826558965
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Trp14Leu
CA397846483
NM_001276695.3:c.41G>T