Canonical Allele Identifier: PA2826872512
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 382991
ClinVar RCV Id: RCV000432283 RCV000886912
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289581.2:p.Pro14Arg
CA7365396
NM_001302652.2:c.41C>G