Canonical Allele Identifier: PA2826464791
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127636
ClinVar RCV Id: RCV000115512 RCV000205979 RCV000212611 RCV000411841 RCV000708836 RCV001194001 RCV001355718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro550Arg
CA019432
NM_001258281.1:c.1649C>G