Canonical Allele Identifier: PA2580544597
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2134032
ClinVar RCV Id: RCV003044729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Ser498Arg
CA8238236
NM_174917.5:c.1494C>G
CA397148245
NM_174917.5:c.1492A>C
CA397148251
NM_174917.5:c.1494C>A