Canonical Allele Identifier: PA2827722305
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 961498
ClinVar RCV Id: RCV001235196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ala412Ser
CA288307335
NM_001353231.2:c.1234G>T