Canonical Allele Identifier: PA2826326256
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230208.1:p.Glu359Lys
CA129707
NM_001243279.3:c.1075G>A