Allele Registry

Canonical Allele Identifier: PA097538

Gene: FSHB HGNC NCBI

ClinVar RCV:

RCV000017628

ClinVar Variation:

16241

HGVS (amino-acid)	Matching Registered Transcripts
NP_000501.1:p.Cys69Gly	CA126288 NM_000510.4:c.205T>G