Canonical Allele Identifier: PA2741884729
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2942560
ClinVar RCV Id: RCV003807726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Leu2158Phe
CA4475982
NM_001458.5:c.6472C>T