Canonical Allele Identifier: PA319804
Gene: TGFBR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 213931
ClinVar RCV Id: RCV000195460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020018.1:p.Pro452Ser
CA319801
NM_001024847.2:c.1354C>T