Canonical Allele Identifier: PA2825968095
Gene: CHAMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 445741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157617.1:p.Ala252Val
CA7070679
NM_001164145.3:c.755C>T