Canonical Allele Identifier: PA1139703080
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 934475
ClinVar RCV Id: RCV001202875 RCV002460135
ClinVar Variation Id: 2562113
ClinVar RCV Id: RCV003310173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ser1156Asn
CA4475050
NM_001458.5:c.3467G>A
CA2580614265
NM_001458.5:c.3465_3467delinsAAA