Canonical Allele Identifier: PA645471490
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408502
ClinVar RCV Id: RCV000465504 RCV000774555 RCV004000782 RCV003129863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn109Ser
CA037887
NM_000251.3:c.326A>G