Allele Registry

Canonical Allele Identifier: PA129704

Gene: ACSF3 HGNC NCBI

ClinVar Variation Id: 31134

HGVS (amino-acid)	Matching Registered Transcripts
NP_777577.2:p.Arg558Trp	CA129703 NM_174917.5:c.1672C>T