Canonical Allele Identifier: PA658660863
Gene: FASN HGNC NCBI

Linked Data

ClinVar Variation Id: 462109
ClinVar RCV Id: RCV000529965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004095.4:p.Ala2453Thr
CA8851028
NM_004104.5:c.7357G>A