Canonical Allele Identifier: PA1139698786
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 654383
ClinVar RCV Id: RCV000810342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Lys198del
CA4178719
NM_001277115.2:c.593_595del
CA366932445
NM_001277115.2:c.586A>T
CA366932451
NM_001277115.2:c.589A>T
CA366932461
NM_001277115.2:c.592A>T