Canonical Allele Identifier: PA2826288055
Gene: TFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 696030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193784.1:p.Met417Leu
CA4386290
NM_001206855.3:c.1249A>T
CA368525748
NM_001206855.3:c.1249A>C