Canonical Allele Identifier: PA2825967919
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 445741
ClinVar RCV Id: RCV000514012 RCV003935350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157616.1:p.Ala252Val
CA7070679
NM_001164144.3:c.755C>T