Canonical Allele Identifier: PA1139672313
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 895595
ClinVar RCV Id: RCV001137782 RCV001137781
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Cys699Ser
CA1652927
NM_000233.4:c.2095T>A
CA346742748
NM_000233.4:c.2096G>C