Canonical Allele Identifier: PA916016811
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11392
ClinVar RCV Id: RCV000012145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Leu686Pro
CA255851
NM_001287344.2:c.2057T>C