Canonical Allele Identifier: PA2826689143
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 955612
ClinVar RCV Id: RCV001228285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271245.1:p.Val224Leu
CA8238225
NM_001284316.2:c.670G>T
CA8238227
NM_001284316.2:c.670G>C