Canonical Allele Identifier: PA915978489
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Phe2690Leu
CA382256941
NM_001377.3:c.8068T>C
CA382256947
NM_001377.3:c.8070C>A
CA382256948
NM_001377.3:c.8070C>G