Canonical Allele Identifier: PA645397367
Gene: TFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 358297
ClinVar RCV Id: RCV000357181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003218.2:p.Ala206Asp
CA4386766
NM_003227.4:c.617C>A