Canonical Allele Identifier: PA1139669657
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 921793
ClinVar RCV Id: RCV001181440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Leu190Phe
CA402949221
NM_000455.5:c.568C>T