Canonical Allele Identifier: PA2741884863
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2921856
ClinVar RCV Id: RCV003782878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val1242Ala
CA369197839
NM_001458.5:c.3725T>C