Canonical Allele Identifier: PA645493162
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 413987
ClinVar RCV Id: RCV000465078 RCV001821320 RCV003970312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Ile389Thr
CA7130468
NM_001099274.3:c.1166T>C