Canonical Allele Identifier: PA2741856165
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 2737285
ClinVar RCV Id: RCV003513680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Trp622Arg
CA413919558
NM_001287344.2:c.1864T>C
CA413919560
NM_001287344.2:c.1864T>A