Allele Registry

Canonical Allele Identifier: PA2825338828

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000002500

RCV000078017

ClinVar Variation:

2399

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Gln260Arg	CA252263 NM_001024946.2:c.779A>G