Allele Registry

Canonical Allele Identifier: PA2825338908

Gene: ASL HGNC NCBI

ClinVar Allele:

17440

ClinVar RCV:

RCV000002502

ClinVar Variation:

2401

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg359Cys	CA339980 NM_001024946.2:c.1075C>T