Canonical Allele Identifier: PA2827718588
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 161709
ClinVar RCV Id: RCV000149245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340142.1:p.Ile592Met
CA174639
NM_001353213.3:c.1776C>G