Canonical Allele Identifier: PA2741856171
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 2585028
ClinVar RCV Id: RCV003340928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Trp668Arg
CA413918378
NM_001287344.2:c.2002T>C
CA413918384
NM_001287344.2:c.2002T>A