Allele Registry

Canonical Allele Identifier: PA2499243976

Gene: CDSN HGNC NCBI

ClinVar RCV:

RCV001648848

ClinVar Variation:

1244640

HGVS (amino-acid)	Matching Registered Transcripts
NP_001255.4:p.Met18Leu	CA3708583 NM_001264.5:c.52A>T CA363317961 NM_001264.5:c.52A>C