Canonical Allele Identifier: PA2825338454
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 3032644
ClinVar RCV Id: RCV003902328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Leu136Pro
CA367639385
NM_001024944.2:c.407T>C