Canonical Allele Identifier: PA341976
Gene: TFR2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003218.2:p.Ala444Thr
CA341975
NM_003227.4:c.1330G>A