Canonical Allele Identifier: PA2826689163
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 967113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271245.1:p.Arg250Trp
CA8238284
NM_001284316.2:c.748C>T