Canonical Allele Identifier: PA645392645
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326894
ClinVar RCV Id: RCV000351589 RCV000391081 RCV000729040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060123.3:p.Arg568Gln
CA8958003
NM_017653.6:c.1703G>A