Canonical Allele Identifier: PA916069742
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 753738
ClinVar RCV Id: RCV000930999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Gln465Arg
CA8238213
NM_174917.5:c.1394A>G