Canonical Allele Identifier: PA233464
Gene: ALG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 166672
ClinVar RCV Id: RCV000152772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001004127.2:p.Phe437Val
CA233463
NM_001004127.2:c.1309T>G