Canonical Allele Identifier: PA2825028318
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_000039.2:p.Leu136Pro
CA367639385
NM_000048.4:c.407T>C