Allele Registry

Canonical Allele Identifier: PA915957148

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000673353

ClinVar Variation:

203627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg146Gln	CA312346 NM_001024946.2:c.437G>A