Canonical Allele Identifier: PA2825968093
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2439941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Gly238Arg
CA388846968
NM_001164145.3:c.712G>A
CA388846969
NM_001164145.3:c.712G>C