Canonical Allele Identifier: PA2825614551
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1754117
ClinVar RCV Id: RCV002364328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ser2148Gly
CA369212779
NM_001127487.2:c.6442A>G