Canonical Allele Identifier: PA2573284936
Gene: ALG12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1430387
ClinVar RCV Id: RCV001967494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077010.1:p.Pro487Leu
CA10300208
NM_024105.4:c.1460C>T