Canonical Allele Identifier: PA2825613185
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1471615
ClinVar RCV Id: RCV001966868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1511Arg
CA369201955
NM_001127487.2:c.4531G>A
CA369201956
NM_001127487.2:c.4531G>C