Canonical Allele Identifier: PA2825967957
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2366818
ClinVar RCV Id: RCV002990630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157616.1:p.Ala401Pro
CA7070763
NM_001164144.3:c.1201G>C