Canonical Allele Identifier: PA1139740418
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 989635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349448.1:p.Glu20Gln
CA332655371
NM_001362519.1:c.58G>C