Canonical Allele Identifier: PA645483265
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 427091
ClinVar RCV Id: RCV000489046 RCV000669138
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Gly280Glu
CA367645418
NM_000048.4:c.839G>A