Canonical Allele Identifier: PA2825029027
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Pro566Arg
CA413920443
NM_000061.3:c.1697C>G