Canonical Allele Identifier: PA2827718696
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326902
ClinVar RCV Id: RCV000334825 RCV000375153 RCV000940130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340143.1:p.Glu191Asp
CA8958333
NM_001353214.3:c.573A>T
CA402509477
NM_001353214.3:c.573A>C