Canonical Allele Identifier: PA645459828
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 231381
ClinVar RCV Id: RCV000216862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.His174Tyr
CA10581003
NM_000455.5:c.520C>T