Canonical Allele Identifier: PA2499237768
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038069
ClinVar RCV Id: RCV001341328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Cys356Tyr
CA389223099
NM_001099274.3:c.1067G>A