Allele Registry

Canonical Allele Identifier: PA2825892329

Gene: LSS HGNC NCBI

ClinVar Allele:

1245986

ClinVar RCV:

RCV001663398

RCV002272485

ClinVar Variation:

1256056

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138908.1:p.Tyr275Cys	CA410520130 NM_001145436.2:c.824A>G