Canonical Allele Identifier: PA2825144658
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3231736
ClinVar RCV Id: RCV004518451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ile424Leu
CA402954156
NM_000455.5:c.1270A>C