Canonical Allele Identifier: PA2825615185
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_001120959.1:p.Met2533Thr
CA369219719
NM_001127487.2:c.7598T>C