Canonical Allele Identifier: PA2573217648
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1382477
ClinVar RCV Id: RCV001890319 RCV004041263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp646Glu
CA369227406
NM_001458.5:c.1938T>A
CA369227407
NM_001458.5:c.1938T>G