Canonical Allele Identifier: PA2827718391
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326894
ClinVar RCV Id: RCV000351589 RCV000391081 RCV000729040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340141.1:p.Arg622Gln
CA8958003
NM_001353212.3:c.1865G>A