Allele Registry

Canonical Allele Identifier: PA658665024

Gene: LEP HGNC NCBI

ClinVar RCV:

RCV000518717

ClinVar Variation:

448905

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