Canonical Allele Identifier: PA2825744274
Gene: BTG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2591105
ClinVar RCV Id: RCV004334905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124386.1:p.Phe10Val
CA9983321
NM_001130914.2:c.28T>G