Canonical Allele Identifier: PA2829867000
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 1500997
ClinVar RCV Id: RCV002017137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060123.3:p.Asn497Asp
CA300365732
NM_017653.6:c.1489A>G