Canonical Allele Identifier: PA2826689167
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_001271245.1:p.Val254Gly
CA312303
NM_001284316.2:c.761T>G