Canonical Allele Identifier: PA343179
Gene: TINF2 HGNC NCBI
ClinVar Allele:
47522
ClinVar RCV:
RCV000032170
ClinVar Variation:
38919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Pro283Ala
CA343178
NM_001099274.3:c.847C>G