Canonical Allele Identifier: PA2829788238
Gene: CNKSR2 HGNC NCBI
ClinVar RCV:
RCV004439872
ClinVar Variation:
3146486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055742.2:p.Ala798Val
CA10366763
NM_014927.5:c.2393C>T