Allele Registry

Canonical Allele Identifier: PA658831385

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000454306

ClinVar Variation:

203613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Arg182Gln	CA312323 NM_001024943.2:c.545G>A