Canonical Allele Identifier: PA2741884784
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2923718
ClinVar RCV Id: RCV003783276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Met2566Thr
CA369219719
NM_001458.5:c.7697T>C