Canonical Allele Identifier: PA916066915
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 423341
ClinVar RCV Id: RCV000481128 RCV001262121 RCV001849382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060936.1:p.Ala81Thr
CA16621181
NM_018466.6:c.241G>A