Canonical Allele Identifier: PA2828102072
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5626
ClinVar RCV Id: RCV000005980 RCV000032168 RCV001382426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Arg247Ser
CA117652
NM_001363668.2:c.739C>A