Allele Registry

Canonical Allele Identifier: PA2825338583

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000002504

RCV000185769

ClinVar Variation:

2403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Arg359Cys	CA252265 NM_001024944.2:c.1075C>T