Canonical Allele Identifier: PA2825611129
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1046054
ClinVar RCV Id: RCV001350561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Phe606Val
CA369227136
NM_001127487.2:c.1816T>G