Allele Registry

Canonical Allele Identifier: PA2828516029

Gene: DYM HGNC NCBI

ClinVar RCV:

RCV000171274

ClinVar Variation:

191094

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361369.1:p.Gly65Asp	CA236000 NM_001374440.1:c.194G>A