Canonical Allele Identifier: PA2499258005
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1046054
ClinVar RCV Id: RCV001350561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Phe606Val
CA369227136
NM_001458.5:c.1816T>G