Canonical Allele Identifier: PA2826561925
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 956854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro18His
CA397841407
NM_001276697.3:c.53C>A
CA645588943
NM_001276697.3:c.53_54delinsAT