Canonical Allele Identifier: PA2825611122
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2953138
ClinVar RCV Id: RCV003810256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Leu604Met
CA369227113
NM_001127487.2:c.1810C>A