Canonical Allele Identifier: PA2573177268
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 1512721
ClinVar RCV Id: RCV002045721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Arg146Pro
CA367639537
NM_001024946.2:c.437G>C