Canonical Allele Identifier: PA1139670610
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 849647
ClinVar RCV Id: RCV001053656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Leu386Pro
CA402953419
NM_000455.5:c.1157T>C