Canonical Allele Identifier: PA2826560351
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1409387
ClinVar RCV Id: RCV001913648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Leu291His
CA397835707
NM_001276695.3:c.872T>A