Canonical Allele Identifier: PA645475525
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237385
ClinVar RCV Id: RCV001366376 RCV002417987 RCV003454700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp748His
CA10582023
NM_000251.3:c.2242G>C