Allele Registry

Canonical Allele Identifier: PA2825338584

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV002624490

ClinVar Variation:

2196834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Arg359Gly	CA4277303 NM_001024944.2:c.1075C>G