Canonical Allele Identifier: PA2825619335
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 234059
ClinVar Variation Id: 2774646
ClinVar RCV Id: RCV003585848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Gly317Arg
CA000803
NM_001126118.1:c.949G>C
CA287485729
NM_001126118.1:c.949G>A