Canonical Allele Identifier: PA658800398
Gene: ALG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 538870
ClinVar RCV Id: RCV000648389 RCV001558426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001004127.2:p.Arg136Cys
CA6989902
NM_001004127.2:c.406C>T