Canonical Allele Identifier: PA334761
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188382
ClinVar RCV Id: RCV000168437 RCV001012659 RCV001034658
ClinVar Variation Id: 1044971
ClinVar RCV Id: RCV001349304 RCV002404828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr557Ser
CA018965
NM_000251.3:c.1670C>G
CA346728048
NM_000251.3:c.1669A>T