Canonical Allele Identifier: PA916016770
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Arg554Gln
CA255831
NM_001287344.2:c.1661G>A