Canonical Allele Identifier: PA2825612565
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1734228
ClinVar RCV Id: RCV002349029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Phe1238Leu
CA369197798
NM_001127487.2:c.3712T>C
CA369197807
NM_001127487.2:c.3714C>A
CA369197809
NM_001127487.2:c.3714C>G