Allele Registry

Canonical Allele Identifier: PA2825338459

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV002045721

ClinVar Variation:

1512721

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Arg146Pro	CA367639537 NM_001024944.2:c.437G>C