Canonical Allele Identifier: PA294296
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 135918
ClinVar RCV Id: RCV000123057 RCV000131151 RCV000585976 RCV002281949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Cys418Trp
CA022547
NM_000455.5:c.1254C>G