Allele Registry

Canonical Allele Identifier: PA645390670

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000406675

RCV000857024

RCV000857025

RCV003153559

ClinVar Variation:

325546

HGVS (amino-acid)	Matching Registered Transcripts
NP_006631.2:p.Ala162Thr	CA8793236 NM_006640.5:c.484G>A