Canonical Allele Identifier: PA916035938
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3370
ClinVar RCV Id: RCV000003537 RCV000034789 RCV000121112 RCV000163302 RCV000232087 RCV000336471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala463Thr
CA159795
NM_001353229.2:c.1387G>A