Canonical Allele Identifier: PA2580111224
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 14399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Val609_Leu610del
CA2580067106
NM_000233.4:c.1824_1829del