Canonical Allele Identifier: PA645476299
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408555
ClinVar RCV Id: RCV000569475 RCV000470535 RCV001844163 RCV001560001 RCV004000795 RCV003470452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu898Ala
CA16610851
NM_000251.3:c.2693A>C