Canonical Allele Identifier: PA2828514642
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 1940745
ClinVar RCV Id: RCV002639485 RCV002658564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361361.1:p.Ser429Leu
CA8958093
NM_001374432.1:c.1286C>T