Canonical Allele Identifier: PA1139704639
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 857613
ClinVar RCV Id: RCV001063326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Trp2164Arg
CA369212668
NM_001458.5:c.6490T>A
CA369212669
NM_001458.5:c.6490T>C