Canonical Allele Identifier: PA645399260
Gene: ACO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374007
ClinVar RCV Id: RCV000415400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001089.1:p.Lys465Asn
CA10257643
NM_001098.3:c.1395G>C
CA411726797
NM_001098.3:c.1395G>T