Canonical Allele Identifier: PA658737927
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491763
ClinVar RCV Id: RCV000583308 RCV001359134 RCV003465307 RCV004002328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val435Leu
CA346724556
NM_000251.3:c.1303G>C