Canonical Allele Identifier: PA2828516555
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_001361372.1:p.Phe396Leu
CA8957965
NM_001374443.1:c.1186T>C
CA402507867
NM_001374443.1:c.1188T>G
CA402507868
NM_001374443.1:c.1188T>A