Canonical Allele Identifier: PA2825614191
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472122
ClinVar RCV Id: RCV000549865 RCV000850350 RCV001770467 RCV004024197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1978Arg
CA369210981
NM_001127487.2:c.5932G>C
CA369210984
NM_001127487.2:c.5932G>A