Canonical Allele Identifier: PA2741813391
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2633438
ClinVar RCV Id: RCV003408511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Leu11Pro
CA1653500
NM_000233.4:c.32T>C