Canonical Allele Identifier: PA094557
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11384
ClinVar RCV Id: RCV000012137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Trp581Arg
CA255835
NM_000061.3:c.1741T>C
CA413919999
NM_000061.3:c.1741T>A