Canonical Allele Identifier: PA2828062711
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 39809
ClinVar RCV Id: RCV000033030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349447.1:p.His359Arg
CA261228
NM_001362518.1:c.1076A>G