Canonical Allele Identifier: PA2826562719
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1409387
ClinVar RCV Id: RCV001913648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Leu171His
CA397835707
NM_001276697.3:c.512T>A