Allele Registry

Canonical Allele Identifier: PA2573076941

Gene: FSHB HGNC NCBI

ClinVar RCV:

RCV000017628

ClinVar Variation:

16241

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369218.1:p.Cys69Gly	CA126288 NM_001382289.1:c.205T>G