Allele Registry

Canonical Allele Identifier: PA112804

Gene: LEP HGNC NCBI

ClinVar RCV:

RCV000015024

ClinVar Variation:

13987

HGVS (amino-acid)	Matching Registered Transcripts
NP_000221.1:p.Arg105Trp	CA123668 NM_000230.3:c.313C>T