Canonical Allele Identifier: PA2827719007
Gene: DYM HGNC NCBI
ClinVar RCV:
RCV004379816
ClinVar Variation:
3086422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340144.1:p.Tyr636Cys
CA8957907
NM_001353215.3:c.1907A>G