Canonical Allele Identifier: PA2825338604
Gene: ASL HGNC NCBI
ClinVar RCV:
RCV001892645
ClinVar Variation:
1383503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Ala378Asp
CA312333
NM_001024944.2:c.1133C>A