Canonical Allele Identifier: PA916001718
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 388124
ClinVar RCV Id: RCV000439994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036193.2:p.Gly32Ala
CA16606518
NM_012063.4:c.95G>C