Canonical Allele Identifier: PA2825338060
Gene: ASL HGNC NCBI
ClinVar RCV:
RCV002248971
ClinVar Variation:
1685244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Ile100Asn
CA4276894
NM_001024943.2:c.299T>A