Canonical Allele Identifier: PA645383330
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 253261
ClinVar RCV Id: RCV000239637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036192.2:p.Gly362Asp
CA10586275
NM_012062.5:c.1085G>A