Canonical Allele Identifier: PA645454331
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Leu586Ser
CA16621156
NM_000061.3:c.1757T>C