Canonical Allele Identifier: PA169976
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142993
ClinVar RCV Id: RCV000132509 RCV000229071 RCV001798461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala417Ser
CA022536
NM_000455.5:c.1249G>T