Canonical Allele Identifier: PA891849838
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 570069
ClinVar RCV Id: RCV000690844
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly605Ser
CA369227120
NM_001458.5:c.1813G>A