Canonical Allele Identifier: PA2826742841
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Leu410Ser
CA16621156
NM_001287345.2:c.1229T>C