Canonical Allele Identifier: PA2580111234
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2221494
ClinVar RCV Id: RCV002657049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Ala689Thr
CA1652938
NM_000233.4:c.2065G>A