Canonical Allele Identifier: PA2828102147
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 857461
ClinVar RCV Id: RCV001063130 RCV002252307 RCV003393833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Met326Val
CA7130501
NM_001363668.2:c.976A>G