Canonical Allele Identifier: PA2828102163
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_001350597.1:p.Ile354Thr
CA7130468
NM_001363668.2:c.1061T>C