Canonical Allele Identifier: PA2825143791
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2853555
ClinVar RCV Id: RCV003617485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ser169Gly
CA402948905
NM_000455.5:c.505A>G