Canonical Allele Identifier: PA1139689322
Gene: KCNJ13 HGNC NCBI

Linked Data

ClinVar Variation Id: 943477
ClinVar RCV Id: RCV001213671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165888.1:p.Pro47Ser
CA351013384
NM_001172417.1:c.139C>T