Canonical Allele Identifier: PA645501998
Gene: COA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 380009
ClinVar RCV Id: RCV000423818 RCV001584118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193570.2:p.Ser16Thr
CA1459916
NM_001206641.3:c.47G>C