Canonical Allele Identifier: PA166962
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141967
ClinVar RCV Id: RCV000130712 RCV000478688 RCV000633343 RCV002247510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ala86Thr
CA000088
NM_000546.6:c.256G>A