Canonical Allele Identifier: PA2825535806
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 575872
ClinVar RCV Id: RCV000698212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Ala339Val
CA389223658
NM_001099274.3:c.1016C>T