Canonical Allele Identifier: PA2825338446
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2202604
ClinVar RCV Id: RCV002630024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Ser133Leu
CA4276941
NM_001024944.2:c.398C>T