Canonical Allele Identifier: PA095191
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91108
ClinVar RCV Id: RCV000076611 RCV001183049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val163Gly
CA021209
NM_000251.3:c.488T>G