Canonical Allele Identifier: PA2825028327
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 1438005
ClinVar RCV Id: RCV001965080
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Ala147Glu
CA367639545
NM_000048.4:c.440C>A