Canonical Allele Identifier: PA916016735
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 35766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.His367Arg
CA260199
NM_001287344.2:c.1100A>G