Canonical Allele Identifier: PA331461
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90887
ClinVar RCV Id: RCV000629808 RCV001190856 RCV001260489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val702Gly
CA020024
NM_000251.3:c.2105T>G