Canonical Allele Identifier: PA2825613129
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1020737
ClinVar RCV Id: RCV001320367 RCV004035004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro1490Ser
CA4475353
NM_001127487.2:c.4468C>T