Canonical Allele Identifier: PA2826464737
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182596
ClinVar RCV Id: RCV000212610 RCV000160636 RCV000462601 RCV000986680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val539Ile
CA019367
NM_001258281.1:c.1615G>A