Canonical Allele Identifier: PA2825338369
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2771347
ClinVar RCV Id: RCV003499454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Glu59Val
CA367638392
NM_001024944.2:c.176A>T