Canonical Allele Identifier: PA645435978
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406577
ClinVar RCV Id: RCV000457955 RCV000573281 RCV001724012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Lys292Arg
CA16615993
NM_001126114.3:c.875A>G