Canonical Allele Identifier: PA2826742813
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Arg386Pro
CA255853
NM_001287345.2:c.1157G>C