Canonical Allele Identifier: PA2825029116
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 852828
ClinVar RCV Id: RCV001057527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Trp634Ser
CA413918362
NM_000061.3:c.1901G>C