Canonical Allele Identifier: PA2825154540
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 1122966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000381.1:p.Ser197Gly
CA10465559
NM_000390.4:c.589A>G