Canonical Allele Identifier: PA2828184251
Gene: MICOS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 3126313
ClinVar RCV Id: RCV004419703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352690.1:p.Tyr127Cys
CA403541282
NM_001365761.2:c.380A>G