Canonical Allele Identifier: PA645421887
Gene: DNAH8 HGNC NCBI

Linked Data

ClinVar Variation Id: 402771
ClinVar RCV Id: RCV000455359 RCV000474097 RCV001265115 RCV003128799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193856.1:p.Thr3924Met
CA3791176
NM_001206927.2:c.11771C>T