Allele Registry

Canonical Allele Identifier: PA2826976808

Gene: SNCB HGNC NCBI

ClinVar RCV:

RCV000007441

RCV002223754

RCV003944805

ClinVar Variation:

7026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304965.1:p.Pro109His	CA118593 NM_001318036.2:c.326C>A