Canonical Allele Identifier: PA2825793304
Gene: TGFB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1405235
ClinVar RCV Id: RCV001903650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129071.1:p.Ser52Arg
CA344725405
NM_001135599.4:c.154A>C
CA344725409
NM_001135599.4:c.156T>A
CA344725410
NM_001135599.4:c.156T>G