Canonical Allele Identifier: PA2825793269
Gene: TGFB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010166
ClinVar RCV Id: RCV001824440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129071.1:p.Ser7Thr
CA344725111
NM_001135599.4:c.20G>C