Canonical Allele Identifier: PA331332
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90713
ClinVar RCV Id: RCV000411811 RCV000506572 RCV000697749 RCV001191249 RCV001800374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn547Ser
CA018784
NM_000251.3:c.1640A>G