Canonical Allele Identifier: PA658672454
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 447700
ClinVar RCV Id: RCV000518619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Asp578Ala
CA346744915
NM_000233.4:c.1733A>C