Canonical Allele Identifier: PA358751
Gene: BTG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225129
ClinVar RCV Id: RCV000210751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006754.1:p.Val141Met
CA358750
NM_006763.3:c.421G>A