Allele Registry

Canonical Allele Identifier: PA915957130

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000002499

ClinVar Variation:

2398

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg95Cys	CA252262 NM_001024946.2:c.283C>T