Canonical Allele Identifier: PA2825535736
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720294
ClinVar RCV Id: RCV002298069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Glu251Gln
CA389226692
NM_001099274.3:c.751G>C