Canonical Allele Identifier: PA2827719375
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1394436
ClinVar RCV Id: RCV001900908
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala67Ser
CA398535118
NM_001353229.2:c.199G>T