Canonical Allele Identifier: PA2825614501
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 857613
ClinVar RCV Id: RCV001063326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Trp2131Arg
CA369212668
NM_001127487.2:c.6391T>A
CA369212669
NM_001127487.2:c.6391T>C