Canonical Allele Identifier: PA2741813393
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2505528
ClinVar RCV Id: RCV003234828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Gly40Cys
CA346815472
NM_000233.4:c.118G>T