Canonical Allele Identifier: PA891850047
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 581971
ClinVar RCV Id: RCV000705929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Cys210Phe
CA402949523
NM_000455.5:c.629G>T