Canonical Allele Identifier: PA2827720970
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3370
ClinVar RCV Id: RCV000003537 RCV000034789 RCV000121112 RCV000163302 RCV000232087 RCV000336471
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala445Thr
CA159795
NM_001353230.2:c.1333G>A