Canonical Allele Identifier: PA181019
Gene: TGFBR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 177927
ClinVar RCV Id: RCV000154587 RCV000777996 RCV002225455 RCV003998253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020018.1:p.Thr180Ile
CA020772
NM_001024847.2:c.539C>T