Allele Registry

Canonical Allele Identifier: PA645412408

Gene: SGCB HGNC NCBI

ClinVar RCV:

RCV000261367

RCV000399677

RCV000543057

RCV002229741

ClinVar Variation:

282248

HGVS (amino-acid)	Matching Registered Transcripts
NP_000223.1:p.Gln11Glu	CA2918525 NM_000232.5:c.31C>G