Canonical Allele Identifier: PA2830358098
Gene: FSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 391834
ClinVar RCV Id: RCV000418908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852111.2:p.Ser242Ile
CA16604316
NM_181446.3:c.725G>T