Canonical Allele Identifier: PA2825614556
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2507108
ClinVar RCV Id: RCV003238999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Tyr2152Asp
CA369212807
NM_001127487.2:c.6454T>G