Allele Registry

Canonical Allele Identifier: PA2825892454

Gene: LSS HGNC NCBI

ClinVar Allele:

1245986

ClinVar RCV:

RCV001663398

RCV002272485

ClinVar Variation:

1256056

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138909.1:p.Tyr206Cys	CA410520130 NM_001145437.2:c.617A>G