Canonical Allele Identifier: PA891850026
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 581784
ClinVar RCV Id: RCV000705710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp176Glu
CA402949017
NM_000455.5:c.528C>A
CA402949022
NM_000455.5:c.528C>G