Allele Registry

Canonical Allele Identifier: PA3057580577

Gene: SHBG HGNC NCBI

ClinVar RCV:

RCV004810831

ClinVar Variation:

3387896

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276045.1:p.Pro69Leu	CA8354296 NM_001289116.2:c.206C>T