Canonical Allele Identifier: PA2826465410
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246035
ClinVar RCV Id: RCV000236402 RCV000686400 RCV001015090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Trp698Gly
CA10584223
NM_001258281.1:c.2092T>G