Canonical Allele Identifier: PA2825611774
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 630832
ClinVar RCV Id: RCV000776836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Asp192Tyr
CA397835843
NM_001126115.1:c.574G>T