Canonical Allele Identifier: PA2579954112
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1778520
ClinVar RCV Id: RCV002398859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Asp57Val
CA397846310
NM_000546.6:c.170A>T