Canonical Allele Identifier: PA2573213124
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1681856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357524.1:p.Glu29Lys
CA7365410
NM_001370595.2:c.85G>A