Canonical Allele Identifier: PA2828880773
Gene: THBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3041153
ClinVar RCV Id: RCV003917280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368868.1:p.Gly677Arg
CA4103063
NM_001381939.1:c.2029G>A
CA366460063
NM_001381939.1:c.2029G>C