Canonical Allele Identifier: PA2826742882
Gene: BTK HGNC NCBI
ClinVar RCV:
RCV000012142
ClinVar Variation:
11389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Met454Lys
CA255846
NM_001287345.2:c.1361T>A