Allele Registry

Canonical Allele Identifier: PA2825338905

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV002624490

ClinVar Variation:

2196834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg353Gly	CA4277303 NM_001024946.2:c.1057C>G