Canonical Allele Identifier: PA2573256727
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501747
ClinVar RCV Id: RCV002042888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036593.2:p.Arg266Gln
CA7130561
NM_012461.2:c.797G>A