Canonical Allele Identifier: PA2825892394
Gene: LSS HGNC NCBI

Linked Data

ClinVar Variation Id: 783884
ClinVar RCV Id: RCV000965494 RCV004535941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138908.1:p.Arg611Gln
CA10074819
NM_001145436.2:c.1832G>A