Canonical Allele Identifier: PA2825226339
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_001001438.1:p.Arg622Gln
CA10074819
NM_001001438.3:c.1865G>A