Canonical Allele Identifier: PA645460004
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403787
ClinVar RCV Id: RCV000464100 RCV001420889 RCV002348256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Thr402Ser
CA045929
NM_000455.5:c.1205C>G
CA402953701
NM_000455.5:c.1204A>T