Canonical Allele Identifier: PA2826563112
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 646725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Pro31Ser
CA397840839
NM_001276698.3:c.91C>T