Canonical Allele Identifier: PA2828102078
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38923
ClinVar RCV Id: RCV000032174 RCV002513292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Thr249Ala
CA343185
NM_001363668.2:c.745A>G