Canonical Allele Identifier: PA2826742803
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Leu366Pro
CA121434
NM_001287345.2:c.1097T>C