Canonical Allele Identifier: PA645459869
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403788
ClinVar RCV Id: RCV000462348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala225Val
CA16616227
NM_000455.5:c.674C>T