Canonical Allele Identifier: PA2828516002
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 3086422
ClinVar RCV Id: RCV004379816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361368.1:p.Tyr579Cys
CA8957907
NM_001374439.1:c.1736A>G