Canonical Allele Identifier: PA2828880967
Gene: THBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3044894
ClinVar RCV Id: RCV003942037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368871.1:p.Ala948Val
CA4102775
NM_001381942.1:c.2843C>T