Canonical Allele Identifier: PA2573080667
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1310649
ClinVar RCV Id: RCV001767763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gln2171Arg
CA369212723
NM_001458.5:c.6512A>G