Canonical Allele Identifier: PA658660874
Gene: FASN HGNC NCBI

Linked Data

ClinVar Variation Id: 462112
ClinVar RCV Id: RCV000532579
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004095.4:p.Glu2478Lys
CA8850985
NM_004104.5:c.7432G>A