Allele Registry

Canonical Allele Identifier: PA103136

Gene: TNC HGNC NCBI

ClinVar RCV:

RCV000083260

ClinVar Variation:

97009

HGVS (amino-acid)	Matching Registered Transcripts
NP_002151.2:p.Thr1796Ser	CA149712 NM_002160.4:c.5386A>T CA374629011 NM_002160.4:c.5387C>G