Canonical Allele Identifier: PA112804
Gene: LEP HGNC NCBI

Linked Data

ClinVar Variation Id: 13987
ClinVar RCV Id: RCV000015024
JSON-LD

Amino-acid Alleles

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