Canonical Allele Identifier: PA645397398
Gene: TFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 415944
ClinVar RCV Id: RCV000471273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003218.2:p.Ile797Val
CA4386139
NM_003227.4:c.2389A>G