Canonical Allele Identifier: PA2828102081
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38924
ClinVar RCV Id: RCV000032175 RCV001818202 RCV001852639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Leu252Pro
CA343187
NM_001363668.2:c.755T>C