Canonical Allele Identifier: PA2825611701
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 848532
ClinVar RCV Id: RCV001052307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Ser182Cys
CA397836031
NM_001126115.1:c.545C>G