Canonical Allele Identifier: PA210238
Gene: PI4K2B HGNC NCBI

Linked Data

ClinVar Variation Id: 208928
ClinVar RCV Id: RCV000201422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060793.2:p.Gln287His
CA210237
NM_018323.4:c.861G>T
CA356533879
NM_018323.4:c.861G>C