Canonical Allele Identifier: PA658670586
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 458018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asn393Ser
CA402953549
NM_000455.5:c.1178A>G