Canonical Allele Identifier: PA1139670806
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 924630
ClinVar RCV Id: RCV001186104
ClinVar Variation Id: 3231735
ClinVar RCV Id: RCV004518450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ser421Arg
CA402954085
NM_000455.5:c.1261A>C
CA402954101
NM_000455.5:c.1263C>A
CA402954105
NM_000455.5:c.1263C>G