Canonical Allele Identifier: PA916016687
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Met35Thr
CA255796
NM_001287344.2:c.104T>C