Canonical Allele Identifier: PA645395967
Gene: DYNC1H1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001367.2:p.Asp338Val
CA10584454
NM_001376.5:c.1013A>T