Canonical Allele Identifier: PA2826569881
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2325373
ClinVar RCV Id: RCV004169282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Met983Leu
CA4179470
NM_001277115.2:c.2947A>C
CA366944762
NM_001277115.2:c.2947A>T