Canonical Allele Identifier: PA2580115727
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730300
ClinVar RCV Id: RCV002326476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asn380Asp
CA402953283
NM_000455.5:c.1138A>G