Canonical Allele Identifier: PA2826742882
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11389
ClinVar RCV Id: RCV000012142
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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