Canonical Allele Identifier: PA916016780
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Arg596Trp
CA255833
NM_001287344.2:c.1786C>T