Canonical Allele Identifier: PA2828516000
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361368.1:p.Val567Met
CA8957911
NM_001374439.1:c.1699G>A