Canonical Allele Identifier: PA1139702693
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 936351
ClinVar RCV Id: RCV001205132 RCV001701305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly876Val
CA166176275
NM_001458.5:c.2627G>T