Canonical Allele Identifier: PA645471385
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 336471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Leu17_Gln18dup
CA1653491
NM_000233.4:c.50_55dup
CA2658995107
NM_000233.4:c.48_49insTTGCAG
CA2658995108
NM_000233.4:c.47_48insCCTGCA