Canonical Allele Identifier: PA645501769
Gene: DNM1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004399.2:p.Ala177Pro
CA170925
NM_004408.4:c.529G>C