Canonical Allele Identifier: PA322682
Gene: TIMM44 HGNC NCBI

Linked Data

ClinVar Variation Id: 215249
ClinVar RCV Id: RCV000198179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006342.2:p.Val194Ile
CA322681
NM_006351.4:c.580G>A