Canonical Allele Identifier: PA2580262671
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1712788
ClinVar RCV Id: RCV002300960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asn1496Asp
CA369201864
NM_001458.5:c.4486A>G