Canonical Allele Identifier: PA645474176
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428531
ClinVar RCV Id: RCV000490918 RCV000704685 RCV001264478 RCV004003471 RCV004527600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg383Gln
CA027092
NM_000251.3:c.1148G>A