Canonical Allele Identifier: PA2825154510
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 989635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000381.1:p.Glu168Gln
CA332655371
NM_000390.4:c.502G>C