Canonical Allele Identifier: PA279239
Gene: PI4K2B HGNC NCBI

Linked Data

ClinVar Variation Id: 208927
ClinVar RCV Id: RCV000201382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060793.2:p.Pro4Thr
CA279238
NM_018323.4:c.10C>A