Allele Registry

Canonical Allele Identifier: PA2825338589

Gene: ASL HGNC NCBI

ClinVar Allele:

17440

ClinVar RCV:

RCV000002502

ClinVar Variation:

2401

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Arg365Cys	CA339980 NM_001024944.2:c.1093C>T