Allele Registry

Canonical Allele Identifier: PA2825566452

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000296085

RCV002229959

RCV003940291

RCV004021715

ClinVar Variation:

325544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001106965.1:p.Arg141Trp	CA8793210 NM_001113493.2:c.421C>T