Canonical Allele Identifier: PA2828102057
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2973758
ClinVar RCV Id: RCV003833332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Arg232Ser
CA257880952
NM_001363668.2:c.696A>C
CA389226195
NM_001363668.2:c.696A>T