Canonical Allele Identifier: PA1139680754
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 856441
ClinVar RCV Id: RCV001061905 RCV004030441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys697Ser
CA346729213
NM_000251.3:c.2089T>A
CA346729215
NM_000251.3:c.2090G>C