Canonical Allele Identifier: PA2825028284
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 3024136
ClinVar RCV Id: RCV003881720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Asp115Tyr
CA4276908
NM_000048.4:c.343G>T