Allele Registry

Canonical Allele Identifier: PA916016736

Gene: BTK HGNC NCBI

ClinVar RCV:

RCV000012121

ClinVar Variation:

11368

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274273.1:p.Tyr368Ser	CA255816 NM_001287344.2:c.1103A>C