Canonical Allele Identifier: PA2741813410
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2621223
ClinVar RCV Id: RCV003385097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Leu607Val
CA1652983
NM_000233.4:c.1819T>G