Canonical Allele Identifier: PA2741884768
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2947425
ClinVar RCV Id: RCV003804055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Phe592Leu
CA369227043
NM_001458.5:c.1774T>C
CA369227047
NM_001458.5:c.1776T>A
CA369227048
NM_001458.5:c.1776T>G