Canonical Allele Identifier: PA915966382
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 827507
ClinVar RCV Id: RCV001027280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ile274Val
CA402950629
NM_000455.5:c.820A>G