Canonical Allele Identifier: PA2825892519
Gene: LSS HGNC NCBI

Linked Data

ClinVar Variation Id: 783884
ClinVar RCV Id: RCV000965494 RCV004535941
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138909.1:p.Arg542Gln
CA10074819
NM_001145437.2:c.1625G>A