Canonical Allele Identifier: PA281899
Gene: TGFB2 HGNC NCBI
ClinVar Allele:
45760
ClinVar RCV:
RCV000030732
ClinVar Variation:
37085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129071.1:p.Pro366His
CA281898
NM_001135599.4:c.1097C>A