Canonical Allele Identifier: PA2741890208
Gene: TNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2542196
ClinVar RCV Id: RCV004307844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002151.2:p.Ala1704Ser
CA5207755
NM_002160.4:c.5110G>T