Canonical Allele Identifier: PA2826565001
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428884
ClinVar RCV Id: RCV000492331 RCV001379190 RCV002289669 RCV004003474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Gly66Ser
CA397844735
NM_001276760.3:c.196G>A