Canonical Allele Identifier: PA645459994
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403786
ClinVar RCV Id: RCV000463119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asn393Thr
CA16616240
NM_000455.5:c.1178A>C