Canonical Allele Identifier: PA2826462818
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91041
ClinVar RCV Id: RCV000221964 RCV000412138 RCV000552261 RCV001353838 RCV001196697 RCV003387753 RCV003997169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu26Val
CA020916
NM_001258281.1:c.76C>G