Canonical Allele Identifier: PA2825922679
Gene: TIMM8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2155890
ClinVar RCV Id: RCV003090783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139423.1:p.Ser5Phe
CA333095753
NM_001145951.2:c.14C>T