Canonical Allele Identifier: PA2827722171
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 253243
ClinVar RCV Id: RCV000239686 RCV003477860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu356Pro
CA10586260
NM_001353231.2:c.1067T>C