Canonical Allele Identifier: PA1139669021
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 947242
ClinVar RCV Id: RCV001218270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp23His
CA402943450
NM_000455.5:c.67G>C