Canonical Allele Identifier: PA3066508707
Gene: FSHR HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000136.2:p.Thr449Ser
CA346767835
NM_000145.4:c.1346C>G
CA346767836
NM_000145.4:c.1345A>T