Canonical Allele Identifier: PA343186
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Thr284Ala
CA343185
NM_001099274.3:c.850A>G