Allele Registry

Canonical Allele Identifier: PA2828513937

Gene: DYM HGNC NCBI

ClinVar Allele:

347101

ClinVar RCV:

RCV000290928

RCV000329327

RCV001753786

RCV003243082

ClinVar Variation:

326892

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361357.1:p.Phe642Leu	CA8957965 NM_001374428.1:c.1924T>C CA402507867 NM_001374428.1:c.1926T>G CA402507868 NM_001374428.1:c.1926T>A