Canonical Allele Identifier: PA2499258156
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1011345
ClinVar RCV Id: RCV001309128 RCV002341620 RCV003314684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr1506Ser
CA369201926
NM_001458.5:c.4516A>T
CA369201928
NM_001458.5:c.4517C>G