Canonical Allele Identifier: PA2826462798
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141032
ClinVar RCV Id: RCV000129363 RCV000212581 RCV000233259 RCV000662735 RCV003997495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser21Cys
CA020808
NM_001258281.1:c.62C>G