Canonical Allele Identifier: PA2826464860
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 183977
ClinVar RCV Id: RCV000163067 RCV000168408 RCV000662475 RCV000759104 RCV001804892 RCV003995232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile567Val
CA019526
NM_001258281.1:c.1699A>G