Allele Registry

Canonical Allele Identifier: PA2741825985

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV003230904

ClinVar Variation:

2503913

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Gly309Arg	CA312329 NM_001024943.2:c.925G>A CA367646131 NM_001024943.2:c.925G>C