Canonical Allele Identifier: PA2580132939
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 1946041
ClinVar RCV Id: RCV002667519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Gly77Arg
CA4276857
NM_001024946.2:c.229G>C