Canonical Allele Identifier: PA658663720
Gene: DNAH8 HGNC NCBI

Linked Data

ClinVar Variation Id: 454566
ClinVar RCV Id: RCV000537231 RCV004023704 RCV003144311 RCV003915475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193856.1:p.Asp1043Glu
CA3788730
NM_001206927.2:c.3129T>A
CA363995613
NM_001206927.2:c.3129T>G