Canonical Allele Identifier: PA2826463559
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187358
ClinVar RCV Id: RCV000167081 RCV000199307 RCV000588197 RCV003468799 RCV003995555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly256Ser
CA022638
NM_001258281.1:c.766G>A