Allele Registry

Canonical Allele Identifier: PA2825338906

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000002504

RCV000185769

ClinVar Variation:

2403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg353Cys	CA252265 NM_001024946.2:c.1057C>T