Canonical Allele Identifier: PA1139766527
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 950969
ClinVar RCV Id: RCV001222795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Arg97Ser
CA397133797
NM_174917.5:c.291G>C
CA397133798
NM_174917.5:c.291G>T