Canonical Allele Identifier: PA658803259
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 527843
ClinVar RCV Id: RCV000632845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Leu140Pro
CA402948248
NM_000455.5:c.419T>C