Canonical Allele Identifier: PA645474687
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229675
ClinVar RCV Id: RCV000220254 RCV000230549 RCV000663329 RCV001358260 RCV001800541 RCV001818514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn583Ile
CA10577984
NM_000251.3:c.1748A>T