Allele Registry

Canonical Allele Identifier: PA2826836754

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000006221

RCV000516514

RCV004018574

ClinVar Variation:

5863

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280624.1:p.Arg87Trp	CA340468 NM_001293695.2:c.259C>T