Canonical Allele Identifier: PA156240
Gene: TBX20 HGNC NCBI

Linked Data

ClinVar Variation Id: 132825
ClinVar RCV Id: RCV000119295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071121.1:p.Met395Arg
CA156238
NM_001077653.2:c.1184T>G