Allele Registry

Canonical Allele Identifier: PA103141

Gene: TNC HGNC NCBI

ClinVar RCV:

RCV000083259

RCV002247481

ClinVar Variation:

97008

HGVS (amino-acid)	Matching Registered Transcripts
NP_002151.2:p.Val1773Met	CA149711 NM_002160.4:c.5317G>A