Canonical Allele Identifier: PA2825631632
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 203601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120686.1:p.Arg469Gln
CA312301
NM_001127214.4:c.1406G>A