Canonical Allele Identifier: PA2828514769
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361362.1:p.Glu191Asp
CA8958333
NM_001374433.1:c.573A>T
CA402509477
NM_001374433.1:c.573A>C