Canonical Allele Identifier: PA2829907880
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 66086
ClinVar RCV Id: RCV000056321 RCV000289979 RCV001256982 RCV001263094 RCV001249505 RCV001849307 RCV002321552 RCV003925015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060936.1:p.Asn107Ser
CA144875
NM_018466.6:c.320A>G