Canonical Allele Identifier: PA2826464708
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224577
ClinVar RCV Id: RCV000210095 RCV000219087 RCV000520524 RCV000530644 RCV000662912 RCV003330582 RCV004541299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu533Ser
CA031393
NM_001258281.1:c.1598T>C