Canonical Allele Identifier: PA109892
Gene: TGFBR2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003233.4:p.Leu308Pro
CA020791
NM_003242.6:c.923T>C