Canonical Allele Identifier: PA2825611099
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 471987
ClinVar RCV Id: RCV000536394 RCV001662580 RCV002413596 RCV002483471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val586Ala
CA4474467
NM_001127487.2:c.1757T>C