Canonical Allele Identifier: PA091649
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 558314
ClinVar RCV Id: RCV000674562
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Arg95His
CA4276865
NM_000048.4:c.284G>A