Canonical Allele Identifier: PA166951
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141963
ClinVar RCV Id: RCV000130708 RCV000255654 RCV000227859 RCV000496787 RCV001257522 RCV003461996 RCV003492603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg26His
CA000227
NM_001126115.1:c.77G>A