Canonical Allele Identifier: PA2826742758
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11366
ClinVar RCV Id: RCV000012119 RCV000768159 RCV001384086 RCV001701564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Arg288Trp
CA255812
NM_001287345.2:c.862C>T