Allele Registry

Canonical Allele Identifier: PA2825307096

Gene: CNMD HGNC NCBI

ClinVar Allele:

3305379

ClinVar RCV:

RCV004439901

ClinVar Variation:

3146515

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011705.1:p.Gln293Pro	CA6993928 NM_001011705.2:c.878A>C