Canonical Allele Identifier: PA2579934522
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 647256
ClinVar RCV Id: RCV000801729
ClinVar Variation Id: 2113149
ClinVar RCV Id: RCV003038628 RCV003477033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ser269Arg
CA397837062
NM_000546.6:c.807C>G
CA397837064
NM_000546.6:c.807C>A
CA397837083
NM_000546.6:c.805A>C