Allele Registry

Canonical Allele Identifier: PA103015

Gene: CHM HGNC NCBI

ClinVar RCV:

RCV000033030

ClinVar Variation:

39809

HGVS (amino-acid)	Matching Registered Transcripts
NP_000381.1:p.His507Arg	CA261228 NM_000390.4:c.1520A>G