Canonical Allele Identifier: PA2825535795
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2914027
ClinVar RCV Id: RCV003647154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Ala323Val
CA389224130
NM_001099274.3:c.968C>T