Allele Registry

Canonical Allele Identifier: PA2825535793

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV003861457

ClinVar Variation:

3006842

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092744.1:p.Met318Ile	CA389224256 NM_001099274.3:c.954G>C CA389224264 NM_001099274.3:c.954G>A CA389224274 NM_001099274.3:c.954G>T