Canonical Allele Identifier: PA2825028278
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 658327
ClinVar RCV Id: RCV000815132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Thr109Met
CA4276902
NM_000048.4:c.326C>T