Allele Registry

Canonical Allele Identifier: PA2825307073

Gene: CNMD HGNC NCBI

ClinVar RCV:

RCV004439893

ClinVar Variation:

3146507

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011705.1:p.Pro15Ser	CA6994220 NM_001011705.2:c.43C>T