Canonical Allele Identifier: PA2829867000
Gene: DYM HGNC NCBI
ClinVar RCV:
RCV002017137
ClinVar Variation:
1500997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060123.3:p.Asn497Asp
CA300365732
NM_017653.6:c.1489A>G