Canonical Allele Identifier: PA916016779
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Leu576Pro
CA121434
NM_001287344.2:c.1727T>C