Canonical Allele Identifier: PA2825631652
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 955612
ClinVar RCV Id: RCV001228285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120686.1:p.Val489Leu
CA8238225
NM_001127214.4:c.1465G>T
CA8238227
NM_001127214.4:c.1465G>C