Canonical Allele Identifier: PA343194
Gene: TINF2 HGNC NCBI
ClinVar Allele:
47530
ClinVar RCV:
RCV000032178
ClinVar Variation:
38927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Arg291Gly
CA343193
NM_001099274.3:c.871A>G