Canonical Allele Identifier: PA2826742795
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Cys351Ser
CA16608702
NM_001287345.2:c.1052G>C
CA413922406
NM_001287345.2:c.1051T>A