Canonical Allele Identifier: PA658679549
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 451799
ClinVar RCV Id: RCV000522967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Gly67Val
CA397840476
NM_001126117.1:c.200G>T