Canonical Allele Identifier: PA2828516391
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 1940745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361371.1:p.Ser281Leu
CA8958093
NM_001374442.1:c.842C>T