Canonical Allele Identifier: PA119688
Gene: LEPR HGNC NCBI

Linked Data

ClinVar Variation Id: 8524
ClinVar Variation Id: 393446
ClinVar RCV Id: RCV000445542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185617.1:p.Lys656Asn
CA119681
NM_001198688.1:c.1968G>C
CA16609263
NM_001198688.1:c.1968G>T