Canonical Allele Identifier: PA2826476870
Gene: LSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1909228
ClinVar RCV Id: RCV002587301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001247418.2:p.Gly6Glu
CA2580096801
NM_001260489.2:c.17_18delinsAA