Canonical Allele Identifier: PA2579912761
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2840193
ClinVar RCV Id: RCV003758430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr238His
CA346732066
NM_000251.3:c.712T>C