Canonical Allele Identifier: PA2825028785
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 944765
ClinVar RCV Id: RCV001215240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Ser289Arg
CA413930025
NM_000061.3:c.867T>A
CA413930030
NM_000061.3:c.867T>G
CA413930053
NM_000061.3:c.865A>C