Canonical Allele Identifier: PA2827722111
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229263
ClinVar RCV Id: RCV004524842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu332Phe
CA398532845
NM_001353231.2:c.994C>T
CA2825002450
NM_001353231.2:c.993_994delinsAT