Canonical Allele Identifier: PA658669178
Gene: CAMK2B HGNC NCBI

Linked Data

ClinVar Variation Id: 430922
ClinVar RCV Id: RCV000516163 RCV000577890 RCV000623203 RCV001003964 RCV001571738 RCV001814167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742076.1:p.Pro139Leu
CA367366362
NM_172079.3:c.416C>T