Canonical Allele Identifier: PA2825975352
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2734542
ClinVar RCV Id: RCV003555090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Tyr1594Ser
CA353352150
NM_001164318.2:c.4781A>C