Canonical Allele Identifier: PA2828514312
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 1040617
ClinVar RCV Id: RCV001344293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361359.1:p.Ser487Asn
CA402506482
NM_001374430.1:c.1460G>A