Canonical Allele Identifier: PA2828102084
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38926
ClinVar RCV Id: RCV000032177
ClinVar Variation Id: 444325
ClinVar RCV Id: RCV000513272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Pro254Ser
CA343191
NM_001363668.2:c.760_761delinsAG
CA389225339
NM_001363668.2:c.760C>T