Canonical Allele Identifier: PA2825976000
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1048081
ClinVar RCV Id: RCV001352899 RCV001871905
ClinVar Variation Id: 1457383
ClinVar RCV Id: RCV001953726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Asp167Glu
CA353333572
NM_001164319.2:c.501C>A
CA353333573
NM_001164319.2:c.501C>G