Allele Registry

Canonical Allele Identifier: PA2825338808

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210606

ClinVar Variation:

224976

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Ser228Arg	CA357217 NM_001024946.2:c.684C>A CA367645177 NM_001024946.2:c.682A>C CA367645181 NM_001024946.2:c.684C>G