Canonical Allele Identifier: PA2825338924
Gene: ASL HGNC NCBI
ClinVar RCV:
RCV001892645
ClinVar Variation:
1383503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Ala372Asp
CA312333
NM_001024946.2:c.1115C>A