Canonical Allele Identifier: PA2826836727
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445583
ClinVar RCV Id: RCV003154992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280624.1:p.Ser55Trp
CA401205740
NM_001293695.2:c.164C>G