Canonical Allele Identifier: PA2828880778
Gene: THBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2276399
ClinVar RCV Id: RCV004128789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368868.1:p.Val791Met
CA4102918
NM_001381939.1:c.2371G>A