Canonical Allele Identifier: PA129708
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31136
ClinVar RCV Id: RCV000024132 RCV000185748 RCV001274019 RCV003415738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Glu359Lys
CA129707
NM_174917.5:c.1075G>A