Canonical Allele Identifier: PA2828101932
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312957
ClinVar RCV Id: RCV000293979 RCV000346506 RCV001042861 RCV003235188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Gln21Arg
CA7130763
NM_001363668.2:c.62A>G