Allele Registry

Canonical Allele Identifier: PA2825566569

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000359029

RCV002229873

ClinVar Variation:

325554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001106965.1:p.Asp341Asn	CA8793637 NM_001113493.2:c.1021G>A