Canonical Allele Identifier: PA916008051
Gene: CHMP2B HGNC NCBI

Linked Data

ClinVar Variation Id: 35472
ClinVar RCV Id: RCV000055937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231573.1:p.Thr63Asn
CA260074
NM_001244644.2:c.188C>A