Canonical Allele Identifier: PA2825028282
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 553111
ClinVar RCV Id: RCV000668492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Arg113Trp
CA4276906
NM_000048.4:c.337C>T