Canonical Allele Identifier: PA2826689152
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1486004
ClinVar RCV Id: RCV002001159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271245.1:p.Ile234Leu
CA397148252
NM_001284316.2:c.700A>C