Canonical Allele Identifier: PA2825967917
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2439941
ClinVar RCV Id: RCV003144841 RCV003164854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157616.1:p.Gly238Arg
CA388846968
NM_001164144.3:c.712G>A
CA388846969
NM_001164144.3:c.712G>C