Canonical Allele Identifier: PA2828102049
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655114
ClinVar RCV Id: RCV000811226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Leu225Val
CA389226409
NM_001363668.2:c.673C>G