Canonical Allele Identifier: PA915956645
Gene: FSHB HGNC NCBI

Linked Data

ClinVar Variation Id: 189329
ClinVar RCV Id: RCV000169745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018090.1:p.Cys100Arg
CA199220
NM_001018080.3:c.298T>C