Canonical Allele Identifier: PA2827061600
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 989635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307888.1:p.Glu20Gln
CA332655371
NM_001320959.1:c.58G>C