Allele Registry

Canonical Allele Identifier: PA2825928662

Gene: SHBG HGNC NCBI

ClinVar RCV:

RCV001598080

RCV003966240

ClinVar Variation:

1222450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139751.1:p.Asp338Asn	CA8354480 NM_001146279.3:c.1012G>A