Canonical Allele Identifier: PA658677674
Gene: COPB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 446713
ClinVar RCV Id: RCV000516154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004757.1:p.Arg254Cys
CA354758675
NM_004766.3:c.760C>T