Canonical Allele Identifier: PA2826742883
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Met454Leu
CA16621155
NM_001287345.2:c.1360A>C
CA413918493
NM_001287345.2:c.1360A>T