Canonical Allele Identifier: PA916016786
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Pro600Arg
CA413920443
NM_001287344.2:c.1799C>G