Canonical Allele Identifier: PA2826559677
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2006345
ClinVar RCV Id: RCV002811698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Asn161His
CA397840460
NM_001276695.3:c.481A>C