Canonical Allele Identifier: PA2573061873
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 1337042
ClinVar RCV Id: RCV001819528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Val596Gly
CA1652990
NM_000233.4:c.1787T>G