Allele Registry

Canonical Allele Identifier: PA2573177268

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV002045721

ClinVar Variation:

1512721

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg146Pro	CA367639537 NM_001024946.2:c.437G>C