Canonical Allele Identifier: PA645396068
Gene: DYNC1H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 408977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001367.2:p.Glu1617Asp
CA16614049
NM_001376.5:c.4851A>C
CA391043659
NM_001376.5:c.4851A>T