Canonical Allele Identifier: PA351545
Gene: CPXM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 221324
ClinVar RCV Id: RCV000207192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937791.2:p.Gly166Glu
CA351544
NM_198148.3:c.497G>A