Canonical Allele Identifier: PA2827722059
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1382962
ClinVar RCV Id: RCV001890669 RCV003355611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Val312Leu
CA398532971
NM_001353231.2:c.934G>T
CA398532972
NM_001353231.2:c.934G>C