Canonical Allele Identifier: PA091635
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 372306
ClinVar RCV Id: RCV000413440 RCV000609637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Arg193Gln
CA4277009
NM_000048.4:c.578G>A