Canonical Allele Identifier: PA312302
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 203601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Arg469Gln
CA312301
NM_174917.5:c.1406G>A