Canonical Allele Identifier: PA915984551
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 650037
ClinVar RCV Id: RCV000805113
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2050Arg
CA369211423
NM_001458.5:c.6148G>A
CA369211425
NM_001458.5:c.6148G>C