Canonical Allele Identifier: PA190556
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184947
ClinVar Variation Id: 823548
ClinVar RCV Id: RCV001019881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp330Glu
CA023397
NM_000455.5:c.990C>G
CA402951635
NM_000455.5:c.990C>A