Allele Registry

Canonical Allele Identifier: PA113072

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015473

RCV000581515

ClinVar Variation:

14394

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Met398Thr	CA123924 NM_000233.4:c.1193T>C