Canonical Allele Identifier: PA2826600528
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 253261
ClinVar RCV Id: RCV000239637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265394.1:p.Gly375Asp
CA10586275
NM_001278465.2:c.1124G>A