Allele Registry

Canonical Allele Identifier: PA2825028592

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV002624490

ClinVar Variation:

2196834

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Arg379Gly	CA4277303 NM_000048.4:c.1135C>G