Canonical Allele Identifier: PA2741884721
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2565527
ClinVar RCV Id: RCV003301931 RCV003777192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys2049Asn
CA369211419
NM_001458.5:c.6147G>C
CA369211421
NM_001458.5:c.6147G>T