Canonical Allele Identifier: PA2827722331
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 860539
ClinVar RCV Id: RCV001066856 RCV004030631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.His423Gln
CA398531676
NM_001353231.2:c.1269C>A
CA398531678
NM_001353231.2:c.1269C>G