Canonical Allele Identifier: PA187608
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184046
ClinVar RCV Id: RCV000163162 RCV000168138 RCV000761079 RCV001264531 RCV001808435 RCV002485009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Gly394Ser
CA022410
NM_000455.5:c.1180G>A