Allele Registry

Canonical Allele Identifier: PA2825566017

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000365616

RCV000890177

RCV001795945

RCV003940292

RCV004021716

ClinVar Variation:

325548

HGVS (amino-acid)	Matching Registered Transcripts
NP_001106963.1:p.Arg237Gln	CA8793269 NM_001113491.2:c.710G>A