Canonical Allele Identifier: PA287495
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 127701
ClinVar RCV Id: RCV000115597 RCV000200053 RCV000213038 RCV002281935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala410Val
CA022505
NM_000455.5:c.1229C>T