Canonical Allele Identifier: PA2825611125
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 570069
ClinVar RCV Id: RCV000690844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly605Ser
CA369227120
NM_001127487.2:c.1813G>A