Canonical Allele Identifier: PA2499258100
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1217431
ClinVar RCV Id: RCV001588104 RCV002471128 RCV002414283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2599Arg
CA369220024
NM_001458.5:c.7795G>A
CA369220025
NM_001458.5:c.7795G>C