Canonical Allele Identifier: PA2825968140
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2257654
ClinVar RCV Id: RCV002783078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Val415Glu
CA7070769
NM_001164145.3:c.1244T>A