Canonical Allele Identifier: PA2826332875
Gene: CHMP2B HGNC NCBI

Linked Data

ClinVar Variation Id: 346806
ClinVar RCV Id: RCV000390491 RCV000516998 RCV003401367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231573.1:p.Thr32Met
CA2500938
NM_001244644.2:c.95C>T