Canonical Allele Identifier: PA1139692121
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 969941
ClinVar RCV Id: RCV001245402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Leu329Pro
CA413929728
NM_001287344.2:c.986T>C