Allele Registry

Canonical Allele Identifier: PA915979596

Gene: SNCB HGNC NCBI

ClinVar RCV:

RCV000007441

RCV002223754

RCV003944805

ClinVar Variation:

7026

HGVS (amino-acid)	Matching Registered Transcripts
NP_003076.1:p.Pro123His	CA118593 NM_003085.5:c.368C>A