Canonical Allele Identifier: PA2829424313
Gene: TFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3176569
ClinVar RCV Id: RCV004474429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003218.2:p.Asn554Asp
CA368526401
NM_003227.4:c.1660A>G