Canonical Allele Identifier: PA2826326354
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230208.1:p.Arg471Trp
CA129709
NM_001243279.3:c.1411C>T