Canonical Allele Identifier: PA2825612516
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1460786
ClinVar RCV Id: RCV001983158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asn1206Lys
CA369197382
NM_001127487.2:c.3618C>A
CA369197384
NM_001127487.2:c.3618C>G