Canonical Allele Identifier: PA109686
Gene: TGFB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224872
ClinVar RCV Id: RCV000210476 RCV001824688 RCV002372209 RCV000255040 RCV004017492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003229.1:p.Arg302Cys
CA354091
NM_003238.6:c.904C>T