Canonical Allele Identifier: PA287499
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 127705
ClinVar RCV Id: RCV000115601 RCV000213021 RCV000476631 RCV001293889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro281Gln
CA023302
NM_000455.5:c.842C>A