Canonical Allele Identifier: PA645475213
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233183
ClinVar RCV Id: RCV000213477 RCV001038410 RCV002510824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn671Asp
CA10577994
NM_000251.3:c.2011A>G