Canonical Allele Identifier: PA094911
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90654
ClinVar RCV Id: RCV000076150 RCV000115501 RCV000148631 RCV000121555 RCV000664309 RCV000986643 RCV001798265 RCV001354246 RCV001719811 RCV002477217 RCV004537290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His46Gln
CA018210
NM_000251.3:c.138C>G
CA346728899
NM_000251.3:c.138C>A