Canonical Allele Identifier: PA2826326352
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31138
ClinVar RCV Id: RCV000024134 RCV001531864 RCV003226167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230208.1:p.Arg471Gln
CA129711
NM_001243279.3:c.1412G>A