Canonical Allele Identifier: PA2826742812
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Arg386Trp
CA255833
NM_001287345.2:c.1156C>T