Allele Registry

Canonical Allele Identifier: PA645420662

Gene: LEP HGNC NCBI

ClinVar Allele:

301797

ClinVar RCV:

RCV000342914

RCV000376522

ClinVar Variation:

358817

HGVS (amino-acid)	Matching Registered Transcripts
NP_000221.1:p.Asp61Asn	CA10623192 NM_000230.3:c.181G>A