Allele Registry

Canonical Allele Identifier: PA915956643

Gene: FSHB HGNC NCBI

ClinVar RCV:

RCV000017628

ClinVar Variation:

16241

HGVS (amino-acid)	Matching Registered Transcripts
NP_001018090.1:p.Cys69Gly	CA126288 NM_001018080.3:c.205T>G