Canonical Allele Identifier: PA216216
Gene: ACLY HGNC NCBI

Linked Data

ClinVar Variation Id: 64470
ClinVar RCV Id: RCV000054657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001087.2:p.Ala916Val
CA216215
NM_001096.3:c.2747C>T