Allele Registry

Canonical Allele Identifier: PA2825353826

Gene: SHBG HGNC NCBI

ClinVar RCV:

RCV001598080

RCV003966240

ClinVar Variation:

1222450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001031.2:p.Asp356Asn	CA8354480 NM_001040.5:c.1066G>A