Canonical Allele Identifier: PA916048526
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 382991
ClinVar RCV Id: RCV000432283 RCV000886912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357524.1:p.Pro14Arg
CA7365396
NM_001370595.2:c.41C>G