Canonical Allele Identifier: PA2826759878
Gene: SHBG HGNC NCBI

Linked Data

ClinVar Variation Id: 1222450
ClinVar RCV Id: RCV001598080 RCV003966240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276043.1:p.Asp298Asn
CA8354480
NM_001289114.2:c.892G>A