Allele Registry

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Canonical Allele Identifier: PA658672732

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479829

ClinVar RCV Id: RCV000574655

ClinVar Variation Id: 491787

ClinVar RCV Id: RCV000584510 RCV000796750 RCV000735960

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln601His	CA346728326 NM_000251.3:c.1803G>C CA346728327 NM_000251.3:c.1803G>T