Canonical Allele Identifier: PA2825535763
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2437094
ClinVar RCV Id: RCV003141014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Thr284Lys
CA389225461
NM_001099274.3:c.851C>A