Allele Registry

Canonical Allele Identifier: PA112860

Gene: SGCB HGNC NCBI

ClinVar RCV:

RCV000009255

ClinVar Variation:

8717

HGVS (amino-acid)	Matching Registered Transcripts
NP_000223.1:p.Leu108Arg	CA119856 NM_000232.5:c.323T>G