Canonical Allele Identifier: PA658813936
Gene: FASN HGNC NCBI

Linked Data

ClinVar Variation Id: 531101
ClinVar RCV Id: RCV000637211 RCV003905718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004095.4:p.Leu2390Arg
CA8851075
NM_004104.5:c.7169T>G