Canonical Allele Identifier: PA2825535769
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1981214
ClinVar RCV Id: RCV002751344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Gly294Ser
CA389225195
NM_001099274.3:c.880G>A