Allele Registry

Canonical Allele Identifier: PA915957140

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000668492

ClinVar Variation:

553111

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg113Trp	CA4276906 NM_001024946.2:c.337C>T