Canonical Allele Identifier: PA913192954
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 631085
ClinVar RCV Id: RCV000777129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Glu351Asp
CA402951830
NM_000455.5:c.1053G>C
CA402951831
NM_000455.5:c.1053G>T