Canonical Allele Identifier: PA188022
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184163
ClinVar RCV Id: RCV000163337 RCV000539118 RCV001731410 RCV003462119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asn412Ser
CA022515
NM_000455.5:c.1235A>G