Canonical Allele Identifier: PA2825338074
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 3024136
ClinVar RCV Id: RCV003881720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Asp115Tyr
CA4276908
NM_001024943.2:c.343G>T