Canonical Allele Identifier: PA2825096532
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 3118611
ClinVar RCV Id: RCV004414975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Phe667Leu
CA1652951
NM_000233.4:c.1999T>C
CA346743296
NM_000233.4:c.2001C>G
CA346743299
NM_000233.4:c.2001C>A