Canonical Allele Identifier: PA2828102068
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5624
ClinVar RCV Id: RCV000005977 RCV000032165 RCV003441705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Lys245Glu
CA117650
NM_001363668.2:c.733A>G