Canonical Allele Identifier: PA2826822936
Gene: CAMK2B HGNC NCBI

Linked Data

ClinVar Variation Id: 493451
ClinVar RCV Id: RCV000584951 RCV003962651 RCV004024658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280099.1:p.Ala536Thr
CA4240050
NM_001293170.2:c.1606G>A