Canonical Allele Identifier: PA2580262514
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2159448
ClinVar RCV Id: RCV003085951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val628Met
CA369227282
NM_001458.5:c.1882G>A