Canonical Allele Identifier: PA915957131
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 558314
ClinVar RCV Id: RCV000674562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Arg95His
CA4276865
NM_001024946.2:c.284G>A