Canonical Allele Identifier: PA916016808
Gene: BTK HGNC NCBI
ClinVar RCV:
RCV000484290
ClinVar Variation:
421091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Met664Leu
CA16621155
NM_001287344.2:c.1990A>C
CA413918493
NM_001287344.2:c.1990A>T