Canonical Allele Identifier: PA658813937
Gene: FASN HGNC NCBI

Linked Data

ClinVar Variation Id: 531092
ClinVar RCV Id: RCV000637202 RCV003965340
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004095.4:p.Ala2398Ser
CA8851070
NM_004104.5:c.7192G>T