Canonical Allele Identifier: PA2828514314
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 1500997
ClinVar RCV Id: RCV002017137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361359.1:p.Asn552Asp
CA300365732
NM_001374430.1:c.1654A>G