Canonical Allele Identifier: PA091627
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 1489478
ClinVar RCV Id: RCV001978315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Arg111Trp
CA159926865
NM_000048.4:c.331C>T