Canonical Allele Identifier: PA916016777
Gene: BTK HGNC NCBI
ClinVar RCV:
RCV000435923
ClinVar Variation:
379335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Cys561Ser
CA16608702
NM_001287344.2:c.1682G>C
CA413922406
NM_001287344.2:c.1681T>A