Canonical Allele Identifier: PA2825535748
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2079474
ClinVar RCV Id: RCV002995401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Gly264Ser
CA389226317
NM_001099274.3:c.790G>A