Canonical Allele Identifier: PA2826463141
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408456
ClinVar RCV Id: RCV000473169 RCV000571885 RCV001526843 RCV004000772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu157Pro
CA16610792
NM_001258281.1:c.470T>C