Allele Registry

Canonical Allele Identifier: PA2829683259

Gene: CNMD HGNC NCBI

ClinVar RCV:

RCV004439893

ClinVar Variation:

3146507

HGVS (amino-acid)	Matching Registered Transcripts
NP_008946.1:p.Pro15Ser	CA6994220 NM_007015.3:c.43C>T