Canonical Allele Identifier: PA2825611783
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Gly193Arg
CA397835820
NM_001126115.1:c.577G>A
CA397835825
NM_001126115.1:c.577G>C