Canonical Allele Identifier: PA645392648
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060123.3:p.Val630Met
CA8957911
NM_017653.6:c.1888G>A