Canonical Allele Identifier: PA1139682173
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 935601
ClinVar RCV Id: RCV001204232 RCV003163542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys871Asn
CA346731125
NM_000251.3:c.2613G>C
CA346731128
NM_000251.3:c.2613G>T