Allele Registry

Canonical Allele Identifier: PA645485331

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000078010

RCV000193312

RCV002514370

RCV003415843

ClinVar Variation:

92360

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Arg12Gln	CA277117 NM_001024943.2:c.35G>A