Allele Registry

Canonical Allele Identifier: PA2826836912

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000359029

RCV002229873

ClinVar Variation:

325554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280624.1:p.Asp329Asn	CA8793637 NM_001293695.2:c.985G>A