Allele Registry

Canonical Allele Identifier: PA091661

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000414625

ClinVar Variation:

372746

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Leu180Arg	CA16042698 NM_000048.4:c.539T>G