Canonical Allele Identifier: PA2825967923
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2644021
ClinVar RCV Id: RCV003411024 RCV003938919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157616.1:p.Arg272Trp
CA7070695
NM_001164144.3:c.814C>T