Canonical Allele Identifier: PA916016731
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Arg341Gly
CA255814
NM_001287344.2:c.1021A>G