Canonical Allele Identifier: PA2826326391
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 203602
ClinVar RCV Id: RCV000185750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230208.1:p.Val519Gly
CA312303
NM_001243279.3:c.1556T>G