Canonical Allele Identifier: PA658811310
Gene: DNAH8 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193856.1:p.Leu194Phe
CA3787975
NM_001206927.2:c.582G>T
CA363985748
NM_001206927.2:c.582G>C