Canonical Allele Identifier: PA1139756833
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 845359
ClinVar RCV Id: RCV001048408 RCV002409416 RCV002481942 RCV003442168 RCV003393808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala60Val
CA8416505
NM_144997.7:c.179C>T