Canonical Allele Identifier: PA915957076
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 203613
ClinVar RCV Id: RCV000454306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Arg182Gln
CA312323
NM_001024944.2:c.545G>A