Canonical Allele Identifier: PA2827717987
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326892
ClinVar RCV Id: RCV000290928 RCV000329327 RCV001753786 RCV003243082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340139.1:p.Phe586Leu
CA8957965
NM_001353210.3:c.1756T>C
CA402507867
NM_001353210.3:c.1758T>G
CA402507868
NM_001353210.3:c.1758T>A