Allele Registry

Canonical Allele Identifier: PA091648

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000002499

ClinVar Variation:

2398

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Arg95Cys	CA252262 NM_000048.4:c.283C>T