Canonical Allele Identifier: PA2741813388
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2633361
ClinVar RCV Id: RCV003391556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Leu10Pro
CA47295578
NM_000233.4:c.29T>C