Canonical Allele Identifier: PA2826326386
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 967113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230208.1:p.Arg515Trp
CA8238284
NM_001243279.3:c.1543C>T