Canonical Allele Identifier: PA645459887
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 231141
ClinVar RCV Id: RCV000223073 RCV001125013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Phe264Tyr
CA10581009
NM_000455.5:c.791T>A