Allele Registry

Canonical Allele Identifier: PA2826759908

Gene: SHBG HGNC NCBI

ClinVar RCV:

RCV001598080

RCV003966240

ClinVar Variation:

1222450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276045.1:p.Asp240Asn	CA8354480 NM_001289116.2:c.718G>A