Canonical Allele Identifier: PA2580376077
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720294
ClinVar RCV Id: RCV002298069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036593.2:p.Glu251Gln
CA389226692
NM_012461.2:c.751G>C