Canonical Allele Identifier: PA2580481758
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2489958
ClinVar RCV Id: RCV003220117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115812.1:p.Pro234Arg
CA388846946
NM_032436.4:c.701C>G