Canonical Allele Identifier: PA2826872513
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 379942
ClinVar RCV Id: RCV000429272 RCV000676910 RCV001553839
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289581.2:p.Pro14Ala
CA7365394
NM_001302652.2:c.40C>G