Canonical Allele Identifier: PA2826476901
Gene: LSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2965560
ClinVar RCV Id: RCV003825710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001247418.2:p.Thr160Met
CA405286438
NM_001260489.2:c.479C>T