Canonical Allele Identifier: PA2741826029
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2577248
ClinVar RCV Id: RCV003324325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Arg146Gly
CA367639529
NM_001024946.2:c.436C>G