Canonical Allele Identifier: PA2499258101
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062847
ClinVar RCV Id: RCV001372611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2644Ala
CA369220523
NM_001458.5:c.7931G>C