Canonical Allele Identifier: PA2828102074
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5625
ClinVar RCV Id: RCV000005978 RCV000005979 RCV001509450 RCV001382425 RCV002490324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Arg247His
CA117651
NM_001363668.2:c.740G>A