Canonical Allele Identifier: PA2573217916
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1473982
ClinVar RCV Id: RCV001969667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys2721Asn
CA369222184
NM_001458.5:c.8163A>C
CA369222188
NM_001458.5:c.8163A>T