Canonical Allele Identifier: PA094362
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 11389
ClinVar RCV Id: RCV000012142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Met630Lys
CA255846
NM_000061.3:c.1889T>A