Canonical Allele Identifier: PA2741839089
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2877319
ClinVar RCV Id: RCV003712837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Met1620Val
CA353352117
NM_001164317.2:c.4858A>G