Canonical Allele Identifier: PA2741817521
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 2769686
ClinVar RCV Id: RCV003578860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000381.1:p.Glu537Gln
CA413787475
NM_000390.4:c.1609G>C