Canonical Allele Identifier: PA2825619508
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Gly350Arg
CA397830162
NM_001126118.1:c.1048G>A
CA397830168
NM_001126118.1:c.1048G>C