Canonical Allele Identifier: PA094472
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Ser14Phe
CA413939745
NM_000061.3:c.41C>T