Canonical Allele Identifier: PA915983132
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 660655
ClinVar RCV Id: RCV000817903 RCV001702722 RCV004028930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp646Asn
CA4474535
NM_001458.5:c.1936G>A