Allele Registry

Canonical Allele Identifier: PA645390683

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000365616

RCV000890177

RCV001795945

RCV003940292

RCV004021716

ClinVar Variation:

325548

HGVS (amino-acid)	Matching Registered Transcripts
NP_006631.2:p.Arg219Gln	CA8793269 NM_006640.5:c.656G>A