Canonical Allele Identifier: PA2828516141
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 161709
ClinVar RCV Id: RCV000149245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361369.1:p.Ile462Met
CA174639
NM_001374440.1:c.1386C>G