Canonical Allele Identifier: PA2825631270
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 203607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120686.1:p.Ala197Thr
CA312312
NM_001127214.4:c.589G>A