Canonical Allele Identifier: PA658665024
Gene: LEP HGNC NCBI

Linked Data

ClinVar Variation Id: 448905
ClinVar RCV Id: RCV000518717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000221.1:p.Leu154Pro
CA369444245
NM_000230.3:c.461T>C