Allele Registry

Canonical Allele Identifier: PA2826837248

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000359029

RCV002229873

ClinVar Variation:

325554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280626.1:p.Asp97Asn	CA8793637 NM_001293697.2:c.289G>A