Canonical Allele Identifier: PA915978306
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Phe2188Leu
CA382248983
NM_001377.3:c.6562T>C
CA382248988
NM_001377.3:c.6564C>A
CA382248989
NM_001377.3:c.6564C>G