Canonical Allele Identifier: PA2828062143
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 1122966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349446.1:p.Ser49Gly
CA10465559
NM_001362517.1:c.145A>G