Allele Registry

Canonical Allele Identifier: PA2825928695

Gene: SHBG HGNC NCBI

ClinVar RCV:

RCV001598080

RCV003966240

ClinVar Variation:

1222450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139753.1:p.Asp241Asn	CA8354480 NM_001146281.3:c.721G>A