Canonical Allele Identifier: PA645493062
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036593.2:p.Arg282Ser
CA117652
NM_012461.2:c.844C>A