Canonical Allele Identifier: PA2828516044
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361369.1:p.Glu115Asp
CA8958333
NM_001374440.1:c.345A>T
CA402509477
NM_001374440.1:c.345A>C