Canonical Allele Identifier: PA658679398
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458567
ClinVar RCV Id: RCV000532028 RCV003409773 RCV004023791 RCV002431551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Cys277Phe
CA001518
NM_001126114.3:c.830G>T