Canonical Allele Identifier: PA658672728
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455526
ClinVar RCV Id: RCV000570637 RCV000588090 RCV000556013 RCV003470712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val598Met
CA031369
NM_000251.3:c.1792G>A