Canonical Allele Identifier: PA915985062
Gene: TNC HGNC NCBI

Linked Data

ClinVar Variation Id: 773511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002151.2:p.Arg1698Gln
CA5207758
NM_002160.4:c.5093G>A