Canonical Allele Identifier: PA2826689130
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271245.1:p.Arg206Trp
CA129709
NM_001284316.2:c.616C>T