Canonical Allele Identifier: PA915957109
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2399
ClinVar RCV Id: RCV000002500 RCV000078017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Gln286Arg
CA252263
NM_001024944.2:c.857A>G