Canonical Allele Identifier: PA113045
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 14406
ClinVar RCV Id: RCV000015487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Leu368Pro
CA123932
NM_000233.4:c.1103T>C