Canonical Allele Identifier: PA2580132943
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2110420
ClinVar RCV Id: RCV003032120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Ser130Pro
CA367639352
NM_001024946.2:c.388T>C