Canonical Allele Identifier: PA2825968098
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1701225
ClinVar RCV Id: RCV002275994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Glu266Lys
CA7070688
NM_001164145.3:c.796G>A