Canonical Allele Identifier: PA2825029038
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 843976
ClinVar RCV Id: RCV001046707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Phe574Leu
CA413920187
NM_000061.3:c.1722C>G
CA413920188
NM_000061.3:c.1722C>A
CA413920203
NM_000061.3:c.1720T>C