Canonical Allele Identifier: PA356389
Gene: TFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219806
ClinVar RCV Id: RCV001853281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003218.2:p.Arg749Gln
CA350771
NM_003227.4:c.2246G>A