Allele Registry

Canonical Allele Identifier: PA2825028324

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV002045721

ClinVar Variation:

1512721

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Arg146Pro	CA367639537 NM_000048.4:c.437G>C