Canonical Allele Identifier: PA2826689207
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_001271245.1:p.Ala303Val
CA8238377
NM_001284316.2:c.908C>T