Canonical Allele Identifier: PA2825968091
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2489958
ClinVar RCV Id: RCV003220117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Pro234Arg
CA388846946
NM_001164145.3:c.701C>G