Canonical Allele Identifier: PA129718
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31141
ClinVar RCV Id: RCV000024137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Met198Arg
CA129717
NM_174917.5:c.593T>G