Canonical Allele Identifier: PA645493070
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036593.2:p.Thr284Ala
CA343185
NM_012461.2:c.850A>G