Allele Registry

Canonical Allele Identifier: PA112878

Gene: SGCB HGNC NCBI

ClinVar RCV:

RCV000009250

RCV000598498

ClinVar Variation:

8712

HGVS (amino-acid)	Matching Registered Transcripts
NP_000223.1:p.Thr151Arg	CA119849 NM_000232.5:c.452C>G