Canonical Allele Identifier: PA2825338328
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 92360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Arg12Gln
CA277117
NM_001024944.2:c.35G>A