Canonical Allele Identifier: PA916016757
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 376203
ClinVar Variation Id: 376204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Cys515Ser
CA16602658
NM_001287344.2:c.1544G>C
CA16602659
NM_001287344.2:c.1543T>A
CA645605194
NM_001287344.2:c.1544_1545delinsCT