Canonical Allele Identifier: PA2828513931
Gene: DYM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361357.1:p.Thr624Ala
CA402507055
NM_001374428.1:c.1870A>G