Canonical Allele Identifier: PA2829331033
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2236824
ClinVar RCV Id: RCV002718847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Met2441Thr
CA353334861
NM_001457.4:c.7322T>C