Canonical Allele Identifier: PA2741933150
Gene: BTG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2591105
ClinVar RCV Id: RCV004334905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006797.3:p.Phe10Val
CA9983321
NM_006806.4:c.28T>G