Canonical Allele Identifier: PA658664807
Gene: DNAH11 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr529Ser
CA4179026
NM_001277115.2:c.1586C>G
CA366936093
NM_001277115.2:c.1585A>T