Canonical Allele Identifier: PA2828102142
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 656147
ClinVar RCV Id: RCV000812488 RCV001816885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Tyr325_Met326insAsnCysTyr
CA7130500
NM_001363668.2:c.968_976dup