Canonical Allele Identifier: PA1139766640
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 992107
ClinVar RCV Id: RCV001280423 RCV002480926 RCV003294180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Ala568Val
CA8238377
NM_174917.5:c.1703C>T