Canonical Allele Identifier: PA2825968128
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2580513
ClinVar RCV Id: RCV003329708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Trp380Arg
CA388847846
NM_001164145.3:c.1138T>C
CA388847847
NM_001164145.3:c.1138T>A