Canonical Allele Identifier: PA2826742833
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11384
ClinVar RCV Id: RCV000012137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Trp405Arg
CA255835
NM_001287345.2:c.1213T>C
CA413919999
NM_001287345.2:c.1213T>A