Canonical Allele Identifier: PA2826393338
Gene: BCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2495406
ClinVar RCV Id: RCV004281171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243327.2:p.Ile140Val
CA382628496
NM_001256398.3:c.418A>G