Canonical Allele Identifier: PA2826836730
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682584
ClinVar RCV Id: RCV002239914 RCV003164340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280624.1:p.Arg57Cys
CA8793147
NM_001293695.2:c.169C>T