Canonical Allele Identifier: PA645474366
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229775
ClinVar RCV Id: RCV000222532 RCV000236848 RCV000473755 RCV000663243 RCV003997770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu489Lys
CA10577978
NM_000251.3:c.1465G>A