Canonical Allele Identifier: PA645394561
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 377889
ClinVar RCV Id: RCV000418627 RCV000812023 RCV003168624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg1159Gln
CA4475052
NM_001458.5:c.3476G>A