Canonical Allele Identifier: PA289269
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 136269
ClinVar RCV Id: RCV000123489 RCV001523135 RCV001274008
ClinVar Variation Id: 1083859
ClinVar RCV Id: RCV001400712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Leu2Pro
CA289268
NM_174917.5:c.5T>C
CA2499223764
NM_174917.5:c.5_6delinsCA