Allele Registry

Canonical Allele Identifier: PA645390667

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000296085

RCV002229959

RCV003940291

RCV004021715

ClinVar Variation:

325544

HGVS (amino-acid)	Matching Registered Transcripts
NP_006631.2:p.Arg130Trp	CA8793210 NM_006640.5:c.388C>T