Canonical Allele Identifier: PA312313
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 203607
ClinVar RCV Id: RCV000185756 RCV002516960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Ala197Thr
CA312312
NM_174917.5:c.589G>A