Canonical Allele Identifier: PA166961
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_001119590.1:p.Ala47Thr
CA000088
NM_001126118.1:c.139G>A