Canonical Allele Identifier: PA2826332912
Gene: CHMP2B HGNC NCBI

Linked Data

ClinVar Variation Id: 260314
ClinVar RCV Id: RCV000249485 RCV000335262 RCV000514690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231573.1:p.Ser146Asn
CA2501038
NM_001244644.2:c.437G>A