Canonical Allele Identifier: PA2827718002
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_001340139.1:p.Val629Met
CA8957911
NM_001353210.3:c.1885G>A