Allele Registry

Canonical Allele Identifier: PA645390701

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000359029

RCV002229873

ClinVar Variation:

325554

HGVS (amino-acid)	Matching Registered Transcripts
NP_006631.2:p.Asp330Asn	CA8793637 NM_006640.5:c.988G>A