Canonical Allele Identifier: PA2826332920
Gene: CHMP2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1654
ClinVar RCV Id: RCV000020696 RCV000084279
ClinVar Variation Id: 2684154
ClinVar RCV Id: RCV003482650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231573.1:p.Gln165His
CA224980
NM_001244644.2:c.495A>C
CA2501045
NM_001244644.2:c.495A>T