Canonical Allele Identifier: PA2825614168
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458571
ClinVar RCV Id: RCV000546011 RCV000563243 RCV001544620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Thr152Ser
CA397836761
NM_001126116.1:c.454A>T