Canonical Allele Identifier: PA658831388
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 372306
ClinVar RCV Id: RCV000413440 RCV000609637
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Arg193Gln
CA4277009
NM_001024943.2:c.578G>A