Canonical Allele Identifier: PA2829330158
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1685823
ClinVar RCV Id: RCV002249990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Pro1603Ser
CA353352205
NM_001457.4:c.4807C>T