Canonical Allele Identifier: PA2741884902
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2933092
ClinVar RCV Id: RCV003790210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro1476Thr
CA166183073
NM_001458.5:c.4426C>A