Canonical Allele Identifier: PA916016729
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11366
ClinVar RCV Id: RCV000012119 RCV000768159 RCV001384086 RCV001701564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Arg322Trp
CA255812
NM_001287344.2:c.964C>T