Canonical Allele Identifier: PA645474789
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265573
ClinVar RCV Id: RCV000256112 RCV000491622 RCV000506471 RCV000629692 RCV003454782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro622Arg
CA10588344
NM_000251.3:c.1865C>G