Allele Registry

Canonical Allele Identifier: PA645483265

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000489046

RCV000669138

ClinVar Variation:

427091

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Gly280Glu	CA367645418 NM_000048.4:c.839G>A