Canonical Allele Identifier: PA658672786
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455531
ClinVar RCV Id: RCV000527808 RCV003584644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile624Val
CA346728479
NM_000251.3:c.1870A>G