Canonical Allele Identifier: PA2826563017
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428883
ClinVar RCV Id: RCV000492745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Val13Gly
CA397841550
NM_001276698.3:c.38T>G