Canonical Allele Identifier: PA091655
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2399
ClinVar RCV Id: RCV000002500 RCV000078017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Gln286Arg
CA252263
NM_000048.4:c.857A>G