Canonical Allele Identifier: PA913195566
Gene: TGFB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 626565
ClinVar RCV Id: RCV000769553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003229.1:p.Met33Arg
CA344725281
NM_003238.6:c.98T>G