Canonical Allele Identifier: PA2825612557
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 661754
ClinVar RCV Id: RCV000819239 RCV002223137 RCV004029002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1232Arg
CA4475101
NM_001127487.2:c.3694G>A
CA369197722
NM_001127487.2:c.3694G>C