Canonical Allele Identifier: PA2826560647
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406597
ClinVar RCV Id: RCV000473145 RCV000492590 RCV000785348 RCV002289602 RCV004000748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg71Leu
CA002845
NM_001276696.3:c.212G>T