Canonical Allele Identifier: PA2825976836
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2877319
ClinVar RCV Id: RCV003712837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Met1589Val
CA353352117
NM_001164319.2:c.4765A>G