Canonical Allele Identifier: PA645487002
Gene: ACLY HGNC NCBI

Linked Data

ClinVar Variation Id: 64470
ClinVar RCV Id: RCV000054657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290203.1:p.Ala970Val
CA216215
NM_001303274.1:c.2909C>T