Canonical Allele Identifier: PA2825338027
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 224970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Glu59Lys
CA357215
NM_001024943.2:c.175G>A