Canonical Allele Identifier: PA2827722062
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529997
ClinVar RCV Id: RCV000635558 RCV002377376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu313Phe
CA398532961
NM_001353231.2:c.939G>T
CA398532962
NM_001353231.2:c.939G>C