Canonical Allele Identifier: PA300028
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 182912
ClinVar RCV Id: RCV001062236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg297Ser
CA023329
NM_000455.5:c.891G>T
CA402951243
NM_000455.5:c.891G>C