Allele Registry

Canonical Allele Identifier: PA2826759854

Gene: SHBG HGNC NCBI

ClinVar RCV:

RCV001598080

RCV003966240

ClinVar Variation:

1222450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276042.1:p.Asp298Asn	CA8354480 NM_001289113.2:c.892G>A