Canonical Allele Identifier: PA2827718392
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2553422
ClinVar RCV Id: RCV003299560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340141.1:p.Thr623Ala
CA402507055
NM_001353212.3:c.1867A>G