Canonical Allele Identifier: PA095099
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753
ClinVar RCV Id: RCV000001823 RCV000076307 RCV000566777 RCV000630204 RCV002460877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro622Leu
CA019478
NM_000251.3:c.1865C>T