Canonical Allele Identifier: PA2826326350
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 203601
ClinVar RCV Id: RCV000185749 RCV000658756 RCV000660548 RCV003977489 RCV004020249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230208.1:p.Arg469Gln
CA312301
NM_001243279.3:c.1406G>A