Canonical Allele Identifier: PA645460023
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 232630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala420Ser
CA046161
NM_000455.5:c.1258G>T