Canonical Allele Identifier: PA170800
Gene: TRMT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 156230
ClinVar RCV Id: RCV000144248 RCV000624590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689505.1:p.Gly206Arg
CA170799
NM_152292.5:c.616G>A
CA357508903
NM_152292.5:c.616G>C