Canonical Allele Identifier: PA2828165242
Gene: TUFM HGNC NCBI

Linked Data

ClinVar Variation Id: 2030878
ClinVar RCV Id: RCV002898699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352289.1:p.Pro160Ser
CA395417591
NM_001365360.2:c.478C>T