Canonical Allele Identifier: PA2828959659
Gene: LSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2965560
ClinVar RCV Id: RCV003825710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372144.1:p.Thr160Met
CA405286438
NM_001385215.1:c.479C>T