Allele Registry

Canonical Allele Identifier: PA2825338390

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210647

ClinVar Variation:

224971

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Glu86Ala	CA357221 NM_001024944.2:c.257A>C