Canonical Allele Identifier: PA103776
Gene: KCNJ13 HGNC NCBI

Linked Data

ClinVar Variation Id: 30332
ClinVar RCV Id: RCV000023267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002233.2:p.Leu241Pro
CA259781
NM_002242.4:c.722T>C