Canonical Allele Identifier: PA1139703279
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 966556
ClinVar RCV Id: RCV001241271 RCV002348821 RCV002480805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg1241His
CA4475107
NM_001458.5:c.3722G>A