Canonical Allele Identifier: PA2826742637
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Ser14Tyr
CA16608230
NM_001287345.2:c.41C>A