Canonical Allele Identifier: PA094098
Gene: BTK HGNC NCBI
ClinVar RCV:
RCV000012141
ClinVar Variation:
11388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Gly613Asp
CA255844
NM_000061.3:c.1838G>A