Canonical Allele Identifier: PA645418781
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 386580
ClinVar RCV Id: RCV000420228 RCV000650340 RCV002356585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093392.1:p.Ala406Val
CA16608244
NM_001099922.3:c.1217C>T