Canonical Allele Identifier: PA645493069
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38921
ClinVar RCV Id: RCV000032172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036593.2:p.Pro283His
CA343182
NM_012461.2:c.848C>A