Canonical Allele Identifier: PA192669
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 185701
ClinVar RCV Id: RCV000165171 RCV003507260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ile361Val
CA022275
NM_000455.5:c.1081A>G