Canonical Allele Identifier: PA916005124
Gene: FASN HGNC NCBI

Linked Data

ClinVar Variation Id: 663774
ClinVar RCV Id: RCV000821724
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004095.4:p.Gly2410Asp
CA8851063
NM_004104.5:c.7229G>A