Canonical Allele Identifier: PA1139706985
Gene: TUFM HGNC NCBI

Linked Data

ClinVar Variation Id: 886835
ClinVar RCV Id: RCV001119244 RCV001856565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003312.3:p.Asn157Ser
CA7985629
NM_003321.5:c.470A>G