Canonical Allele Identifier: PA2826326388
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 972111
ClinVar RCV Id: RCV001248069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230208.1:p.Ala518Asp
CA8238286
NM_001243279.3:c.1553C>A