Canonical Allele Identifier: PA2828102115
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2914027
ClinVar RCV Id: RCV003647154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Ala288Val
CA389224130
NM_001363668.2:c.863C>T