Allele Registry

Canonical Allele Identifier: PA2826837078

Gene: SEPTIN9 HGNC NCBI

ClinVar RCV:

RCV000359029

RCV002229873

ClinVar Variation:

325554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280625.1:p.Asp124Asn	CA8793637 NM_001293696.2:c.370G>A