Canonical Allele Identifier: PA1139670101
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 932401
ClinVar RCV Id: RCV001200180
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Ser298Ile
CA367645682
NM_001024944.2:c.893G>T