Canonical Allele Identifier: PA331708
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91245
ClinVar RCV Id: RCV000076750 RCV000491370 RCV001052685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu310Pro
CA022549
NM_000251.3:c.929T>C