Canonical Allele Identifier: PA916016697
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Arg62His
CA255794
NM_001287344.2:c.185G>A