Canonical Allele Identifier: PA2827349271
Gene: CNKSR2 HGNC NCBI
ClinVar RCV:
RCV004439872
ClinVar Variation:
3146486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317699.1:p.Ala749Val
CA10366763
NM_001330770.2:c.2246C>T