Canonical Allele Identifier: PA2828102081
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Leu252Pro
CA343187
NM_001363668.2:c.755T>C