Canonical Allele Identifier: PA916016811
Gene: BTK HGNC NCBI
ClinVar RCV:
RCV000012145
ClinVar Variation:
11392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Leu686Pro
CA255851
NM_001287344.2:c.2057T>C