Allele Registry

Canonical Allele Identifier: PA118594

Gene: SNCB HGNC NCBI

ClinVar RCV:

RCV000007441

RCV002223754

RCV003944805

ClinVar Variation:

7026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001502.1:p.Pro123His	CA118593 NM_001001502.3:c.368C>A