Canonical Allele Identifier: PA1139703445
Gene: FASN HGNC NCBI

Linked Data

ClinVar Variation Id: 849274
ClinVar RCV Id: RCV001053201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004095.4:p.Val2474Ile
CA8850988
NM_004104.5:c.7420G>A