Canonical Allele Identifier: PA2825028495
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2282358
ClinVar RCV Id: RCV002831185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Asn289Thr
CA4277163
NM_000048.4:c.866A>C