Canonical Allele Identifier: PA645392647
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 284211
ClinVar RCV Id: RCV000321281 RCV000353342 RCV000378341 RCV004021154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060123.3:p.Gln593Arg
CA8957962
NM_017653.6:c.1778A>G