Canonical Allele Identifier: PA2828102037
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38916
ClinVar RCV Id: RCV000032164 RCV000394153 RCV000545340 RCV000350321 RCV001269497 RCV001731323 RCV002496488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Ser210Tyr
CA343172
NM_001363668.2:c.629C>A