Canonical Allele Identifier: PA129710
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Arg471Trp
CA129709
NM_174917.5:c.1411C>T