Canonical Allele Identifier: PA916035850
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529980
ClinVar RCV Id: RCV000635536 RCV003478357 RCV004025463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu321Gly
CA8416196
NM_001353229.2:c.962A>G