Allele Registry

Canonical Allele Identifier: PA236001

Gene: DYM HGNC NCBI

ClinVar RCV:

RCV000171274

ClinVar Variation:

191094

HGVS (amino-acid)	Matching Registered Transcripts
NP_060123.3:p.Ser141Asn	CA236000 NM_017653.6:c.422G>A