Canonical Allele Identifier: PA1139692119
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 944765
ClinVar RCV Id: RCV001215240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Ser323Arg
CA413930025
NM_001287344.2:c.969T>A
CA413930030
NM_001287344.2:c.969T>G
CA413930053
NM_001287344.2:c.967A>C