Canonical Allele Identifier: PA2825631238
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 446065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120686.1:p.Pro182Leu
CA8237688
NM_001127214.4:c.545C>T