Allele Registry

Canonical Allele Identifier: PA093629

Gene: BTK HGNC NCBI

ClinVar Allele:

26426

ClinVar RCV:

RCV000012140

ClinVar Variation:

11387

HGVS (amino-acid)	Matching Registered Transcripts
NP_000052.1:p.Ala607Asp	CA255842 NM_000061.3:c.1820C>A