Canonical Allele Identifier: PA2825968124
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1702634
ClinVar RCV Id: RCV002278952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Pro361Leu
CA388847734
NM_001164145.3:c.1082C>T