Canonical Allele Identifier: PA2826689204
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271245.1:p.Arg293Trp
CA129703
NM_001284316.2:c.877C>T