Canonical Allele Identifier: PA2826689151
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2233742
ClinVar RCV Id: RCV002718090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271245.1:p.Ile234Val
CA397148253
NM_001284316.2:c.700A>G