Canonical Allele Identifier: PA166351
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141764
ClinVar RCV Id: RCV000130398 RCV000413074 RCV000538977 RCV000763416 RCV001255676 RCV002247507 RCV002288637 RCV003149899 RCV003460927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Arg135Trp
CA000423
NM_001126116.1:c.403C>T