Canonical Allele Identifier: PA916016794
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 654423
ClinVar RCV Id: RCV000810388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274273.1:p.Met621Leu
CA413919573
NM_001287344.2:c.1861A>T
CA413919581
NM_001287344.2:c.1861A>C