Canonical Allele Identifier: PA2825615170
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 644009
ClinVar RCV Id: RCV000797842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Cys2522Ser
CA369219569
NM_001127487.2:c.7564T>A
CA369219576
NM_001127487.2:c.7565G>C