Canonical Allele Identifier: PA2826689140
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 717381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271245.1:p.Ala221Thr
CA8238224
NM_001284316.2:c.661G>A