Canonical Allele Identifier: PA111000
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 188348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp194Asn
CA023091
NM_000455.5:c.580G>A