Canonical Allele Identifier: PA645392646
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_060123.3:p.Phe587Leu
CA8957965
NM_017653.6:c.1759T>C
CA402507867
NM_017653.6:c.1761T>G
CA402507868
NM_017653.6:c.1761T>A