Canonical Allele Identifier: PA322413
Gene: TGFB2 HGNC NCBI
ClinVar Allele:
209443
ClinVar RCV:
RCV000197949
ClinVar Variation:
213846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129071.1:p.Cys346Phe
CA322411
NM_001135599.4:c.1037G>T