Canonical Allele Identifier: PA2826836725
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682581
ClinVar RCV Id: RCV002239911 RCV004045120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280624.1:p.Ser55Leu
CA8793142
NM_001293695.2:c.164C>T