Canonical Allele Identifier: PA2825338132
Gene: ASL HGNC NCBI
ClinVar Allele:
359814
ClinVar RCV:
RCV000414625
ClinVar Variation:
372746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Leu180Arg
CA16042698
NM_001024943.2:c.539T>G