Canonical Allele Identifier: PA129716
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Pro243Leu
CA129715
NM_174917.5:c.728C>T