Canonical Allele Identifier: PA2826742847
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 2737285
ClinVar RCV Id: RCV003513680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274274.1:p.Trp412Arg
CA413919558
NM_001287345.2:c.1234T>C
CA413919560
NM_001287345.2:c.1234T>A