Canonical Allele Identifier: PA2825338846
Gene: ASL HGNC NCBI
ClinVar RCV:
RCV003230904
ClinVar Variation:
2503913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Gly283Arg
CA312329
NM_001024946.2:c.847G>A
CA367646131
NM_001024946.2:c.847G>C