Allele Registry

Canonical Allele Identifier: PA2825566134

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000406675

RCV000857024

RCV000857025

RCV003153559

ClinVar Variation:

325546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001106964.1:p.Ala16Thr	CA8793236 NM_001113492.2:c.46G>A