Canonical Allele Identifier: PA2828102089
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1981214
ClinVar RCV Id: RCV002751344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Gly259Ser
CA389225195
NM_001363668.2:c.775G>A