Canonical Allele Identifier: PA645493061
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036593.2:p.Arg282His
CA117651
NM_012461.2:c.845G>A