Canonical Allele Identifier: PA916048525
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 379942
ClinVar RCV Id: RCV000429272 RCV000676910 RCV001553839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357524.1:p.Pro14Ala
CA7365394
NM_001370595.2:c.40C>G