Canonical Allele Identifier: PA165862
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141585
ClinVar RCV Id: RCV000130169 RCV000198710 RCV000520077 RCV003460914 RCV003997554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn835Asp
CA020655
NM_000251.3:c.2503A>G