Canonical Allele Identifier: PA2827718618
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326889
ClinVar RCV Id: RCV000299929 RCV000357111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340142.1:p.Val684Met
CA8957911
NM_001353213.3:c.2050G>A