Canonical Allele Identifier: PA189927
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 184745
ClinVar RCV Id: RCV000164055 RCV000197833 RCV000485066 RCV000780790 RCV000989701 RCV001294069 RCV003407609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Arg333Cys
CA000530
NM_001126112.3:c.997C>T