Canonical Allele Identifier: PA2741984949
Gene: ALG12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2871879
ClinVar RCV Id: RCV003608460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077010.1:p.Val395Leu
CA412072099
NM_024105.4:c.1183G>T
CA412072100
NM_024105.4:c.1183G>C