Allele Registry

Canonical Allele Identifier: PA2825338422

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV001978315

ClinVar Variation:

1489478

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Arg111Trp	CA159926865 NM_001024944.2:c.331C>T