Canonical Allele Identifier: PA645454316
Gene: BTK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000052.1:p.Cys527Ser
CA16608702
NM_000061.3:c.1580G>C
CA413922406
NM_000061.3:c.1579T>A