Canonical Allele Identifier: PA2825535775
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713990
ClinVar RCV Id: RCV002296973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Lys302Asn
CA389224890
NM_001099274.3:c.906G>T
CA389224895
NM_001099274.3:c.906G>C