Canonical Allele Identifier: PA2741856168
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 2745641
ClinVar RCV Id: RCV003511585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Ala645Asp
CA413918959
NM_001287344.2:c.1934C>A